With proper treatment, these patients can be productive and active members of the main stream of society. Enter a Crossword Clue. Results. Pierre Robin syndrome: A birth defect characterized by abnormalities in the facial bones, resulting in a smaller-than-normal lower jaw or receding chin. Restoration of 16, 26, 36, 46, 47 was done with composite and pit and fissure sealants were applied on 44, 34, 24, 14, 15, 25; [Table/Fig-1f]. Multiple synostoses in the sutures of the cranial base in this syndrome result in the hypoplasia of the midface, shallow orbits, a short nasal dorsum, maxillary hypoplasia, and, in severe cases,. Crouzon syndrome exhibits considerable phenotypic heterogeneity, in the aetiology of which genetics play an important role. His eye sockets were shallow causing the eyes to appear very bulging. Crouzon syndrome (CS) is a rare genetic disorder characterized by premature closure of one or more cranial sutures and produces the characteristic craniofacial and other associated abnormalities. Signs and symptoms of Crouzon syndrome may include wide-set, bulging eyes; strabismus (misalignment of the eyes); a small, "beak-shaped" nose; and an. The therapy of patients with Crouzon syndrome involves a multidisciplinary team. The Crossword Solver found 30 answers to "jutting part of lower jaw (4)", 4 letters crossword clue. Enter the length or pattern for better results. Defects in any of these genes can result in premature fusion of the bones in the skull. 3%, 5. In this case full orthodontic pre-surgical preparation with fixed appliances was carried out. Maxillary dental crowding is also common in Crouzon patients (Helman et al. Introduction. Crouzon a French neurologist first described the condition in an earlier part of the 20th century. 0000000000000946. Next step would be to visit the level’s master topic to find the answers of the other clues : Figgerits Rare Level 28. The pathogenesis of craniofacial anomalies frequently involves defects in the migration, proliferation, and fate of neural crest cells destined for the craniofacial skeleton. Crouzon syndrome is a genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting in the skull and facial deformities. Crossword Clue" Puns Are A Rare Medium Well Done" (Dad Joke) Crossword Clue;. Sort by Length. Please remember that I’ll always mention the master topic of the game :. Recent seen on March 12, 2021 we are everyday update LA Times Crosswords, New York Times Crosswords and many more. Crouzon syndrome is a rare inherited disorder in which many of the flexible seams (sutures) in a baby’s skull turn to bone and fuse too early. Severity of the syndrome varies from mild to severe among individuals. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Many features of Crouzon syndrome result from the premature fusion of the skull bones. Summarize the treatment of Crouzon syndrome. The Fgfr2c C342Y mutation results in. 0As mentioned in the definition, Crouzon syndrome is a genetic disease whose origin resides on the “FGFR2” gene where there is "error" or "mutation". Cycloplegic refraction was +1. And I have to say that Figgerits is a crossword reinvention. igenetics also plays an important role in Crouzon syndrome [2,4]. Enter the length or pattern for better results. Rhinoplasty. Crouzon syndrome. Telephone interviews were carried out with eight informants and data were analysed according to grounded theory. Oral surgery: to align the teeth of the upper and lower jaws. G. Abstract. Not the regular crosswords with the same graphics and gameplay, but a new way. Early fusion of the skull is the hallmark of a. 1083A>G and c. 42 The term “Crouzon syndrome” describes an autosomal disease, which results from hereditary mutations identified in specific genes in the human DNA chain. For instance, in the case of syndromic synostosis (e. 4:1 has been reported. Thus your lower jaw also grows extensively, causing Mandibular Prognathism. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Small lower jaw (micrognathia). Pathology Features include: abnormal calvarial shape: in severe case can give a "cloverleaf skull" shallow orbits with exo. Crouzon syndrome (OMIM: 123500) is caused by mutations in FGFR2, mapped to chromosome locus 10q26. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Click the answer to find similar crossword clues . ) What is Crouzon Syndrome? Crouzon syndrome is one of several types of craniosynostosis – a condition that results from the premature fusion of one or more of the seams (sutures) of the skull bones. His bone age. How Is Crouzon Syndrome. His parents are General Physicians practicing in Iraq. Crouzon syndrome (OMIM: 123500) is caused by mutations in FGFR2, mapped to chromosome locus 10q26. The tongue often falls back in the throat, causing. tip of lower jaw Crossword Clue. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. This early fusion prevents the skull from growing normally and affects the shape of the head and face. Craniofacial developmental anomalies are the most common source of birth defects in humans, present in 1 out of 700 births [1–3]. The babies that have Crouzon syndrome can present the following symptoms: • Bulging eyeballs • Enlarged forehead Crouzon syndrome is a genetic condition that results in an abnormal fusion of some of the bones of the skull and face that does not allow the bones to grow normally, affecting the shape of the head, the appearance of the face and the relationship of the teeth. Answers for The protruding part of the lower jaw (4) crossword clue, 4 letters. Patient care necessitates multifaceted specialization and management. wide-set, bulging eyes. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Widens the upper jaw, derotates the orbits, and narrows the upper face. The bones around the eyes (orbits) are wider spaced and shallower than usual, causing the eyes to bulge outwards. loyal. A positive result should prompt a careful neurosurgical assessment as hydrocephalus is a frequent association. The Crossword Solver found 30 answers to "Jaw bone (8)", 8 letters crossword clue. Crouzon syndrome is a rare genetic disorder that affects about 1 in 50,000 babies. Techniques to encourage bone growth may be used. We found 20 possible solutions for this clue. Pronunciation of Crouzon syndrome with 2 audio pronunciations and more for Crouzon syndrome. Lower jaw. 13. 8 years. All synonyms & crossword answers with 3-11 Letters for JAW found in daily crossword puzzles: NY Times, Daily Celebrity, Telegraph, LA Times and more. In Crouzon syndrome, certain bones in the skull fuse too soon. Premature fusion of the skull bones prevents the skull from growing normally and affects the shape of the child’s head and face. Crouzon syndrome, with a prevalence of 1:60,000 [], in most cases results from a mutation of the FGFR2 gene, which is either inherited in an autosomal dominant manner or arises as a de novo mutation, as in 30–60% of cases [2,3,4,5]. 1,6,16. Signs and symptoms of Crouzon syndrome may include wide-set, bulging eyes; strabismus (misalignment of the eyes); a small, "beak-shaped" nose. which results in hydrocephalus and venous dilation of the. The Crossword Solver found 30 answers to "lower jaw", 8 letters crossword clue. Since the branchial arches are important developmental features in a growing embryo, disturbances in their development. [ 1, 3, 6] Bony face deformity is observed at birth, followed with time by other factors of the syndrome. Crouzon syndrome is an autosomal dominant condition primarily characterized by craniosynostosis. The prognathism may have its origin in hereditary conditions, such as Crouzon syndrome whose condition causes a rare facial appearance as wide nose, thick and prominent eyebrows, eyes widely separated and prominent jaw. Crouzon syndrome is an autosomal dominant disorder characterized by craniosynostosis causing secondary alterations of the facial bones and facial structure. The Sun Coffee Time Crossword; Last Seen Dates. This is usually performed during the teen years. Click the answer to find similar crossword clues . Lord H, Lester T, Hoogeboom AJ, et al. The severity of these signs and symptoms varies among affected people. Ophthalmologists should be aware of the many ophthalmic associations in Crouzon syndrome and must be alert toward conditions that may require early intervention. Frequency Crouzon syndrome with acanthosis nigricans is rare; this condition occurs in about 1Crouzon syndrome (CS) is an autosomal dominant disorder characterized by craniofacial deformities caused by the early closure of cranial sutures. headdress. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Although the mandible, or lower jaw, grows normally and because the maxilla is retruded, it causes the lower jaw to appear enlarged or more prominent. It was last seen in The Daily Telegraph quick crossword. Symptoms. Enter a Crossword Clue. Click the answer to find similar crossword clues . Skull reshaping may need to be repeated as the child grows to give the best possible results. This results in the slowing or halting of theCrouzon syndrome is a compound craniofacial disorder that presents with a myriad of multisystem anomalies and bony abnormalities. Jaw deformities such as a receding upper jaw or a protruding lower jaw. Bone deformities in the middle of the face. A female-to-male sex ratio of 2. Indeed, mutations in the FGFR2 gene have been detected in more than 50% of patients with Crouzon syndrome. Solve your "jaw" crossword puzzle fast & easy with the-crossword-solver. Learn about Crouzon Syndrome, including symptoms, causes, and treatments. 25Crouzon syndrome (CS) is member of a group of disorders involving craniosynostosis. Upper jaw. The surgeon will use metal plates and screws to hold the jaw in its new position. Click the answer to find similar crossword clues . The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. JAW, lower (60%) JAW part (60%) jaw muscle (60%) jaw bone (60%. Other abnormalities associated with the syndrome include having a prominent lower jaw, hearing and spinal problems. ) Figgerits and the link to the main level Figgerits answers level 28. 8% of all craniosynostoses []. Sort by Length. Refine the search results by specifying the number of letters. The Crouzon syndrome is named after the French neurologist, Octave Crouzon, who described this disorder [1–3] which includes a triad of skull deformities, facial anomalies, and an exopthalmus [4, 5]. Objective. Enter the length or pattern for better results. The Crossword Solver found 30 answers to "front of lower jaw 4", 4 letters crossword clue. 8% of all cases of craniosynostosis. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Click the answer to find similar crossword clues. Mayo Clinic notes this type of procedure is appropriate for children once their jaw growth stops, at about 14 to 16 years of age for females and 17 to 21 for males. Researchers sorted normal faces according to how. Outline the workup of Crouzon. Search for crossword clues found in the Daily Celebrity, NY Times, Daily Mirror, Telegraph and major publications. , 1994; Glaser et al. Crouzon Syndrome is a genetic disorder marked by the premature fusion of certain skull bones during a child's development. Crowded teeth. 13), which was deeper than that. Representation in media — like Selma Blair's openness about her MS — also goes a long way. This can result in prognathism or other head and facial irregularities. Learn about Crouzon Syndrome, including symptoms, causes, and treatments. Glaucoma with Crouzon Syndrome. Enter the length or pattern for better results. It is associated with Crouzon syndrome, Angelman syndrome, as well as Fetal alcohol syndrome. 8% of all cases of. It is the most common type of syndromic craniosynostosis. Description. Crouzon syndrome. This means premature fusion of the fibrous joints (called sutures) between certain bones. Deciduous canines and the left lateral incisor were present in the lower jaw, and the permanent canines, the left lateral incisor, and the lower right third molar were impacted. This is a genetic syndrome that causes the seams of your skull to fuse abnormally. It meant we were born with bulging eyes. The small, poorly developed upper jaw. Deformed or misshapen head with the head being wide across the front and short from front to back; Bulging wide-set eyes; Facial bone deformities; Jaw deformities like a protruding lower jaw; Sleep Apnea; Problems breathing due to facial deformities caused by Crouzon Syndrome. The syndrome was first described in 1912 by French physician Octave Crouzon when he identified both a mother and daughter with what was originally called. The aim of this study was to explore the difference in maxillary and mandibular morphology and spatial position in Asian and Caucasian Crouzon syndrome patients. A female-to-male sex ratio of 2. Crouzon syndrome atau sindrom Crouzon adalah kelainan genetik yang ditandai dengan penggabungan dini tulang tengkorak tertentu ( craniosynostosis ). This is a rare condition affecting 60 people in 1 million people. 1% in blood. FGFR2 mediates extracellular signals into cells and the mutations in the FGFR2 gene cause this syndrome occurrence. Crouzon syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). Lower jaw. We report a rare case of Crouzon syndrome in a very young infant with distinct features of craniofacial malformations. In ophthalmology, ocular involvement can include variations ranging from exophthalmos and divergent strabismus to ocular hypertelorism []. concave profile with an asymmetric mandibular jaw line. Gene mutations are responsible for the abnormal skull fusions. The hallmarks of Crouzon syndrome are overcrowding of upper and lower teeth, V-shaped maxillary dental arch, and bulging mandible (lower jaw). GARD: 19 Crouzon syndrome is a disorder characterized by early fusion of certain skull bones (craniosynostosis). Result Crossword Clue Answers. , 2005 ). Learn about Crouzon Syndrome, including symptoms, causes, and treatments. Le Fort 1 surgery may be recommended when the upper jaw is under-developed, which results in the upper teeth being positioned behind the lower teeth. This prevents normal growth of the skull, which can affect the shape of the head and face. Click the answer to find similar crossword clues . It makes up approximately 4. C H I N. [1 2] It is one of the craniosynostosis syndrome that is caused by a mutation in the fibroblast growth factor receptor 2 gene. Its mutation will therefore cause a acceleration of the ossification process of all. The Fgfr2cC342Y/+ Crouzon syndrome mouse model carries a cysteine to tyrosine substitution at amino acid position 342 (Cys342Tyr; C342Y) in fibroblast growth factor receptor 2 (FGFR2), equivalent to the FGFR2 mutation commonly associated with Crouzon syndrome. The bones around the eyes (orbits) are wider spaced and shallower than usual, causing the eyes to bulge outwards. Lower jaw protruding. Short forearms (missing radius bone) and short range of motion at the elbow. Visual acuity is reduced. 1 Craniosynostosis is the premature fusion of the skull bones. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Once Crouzon syndrome is suspected, advanced imaging methods such as three-dimensional computed tomography must be requested, showing early signs of cranial sutures fusion. Find clues for The protruding part of the lower jaw (4) or most any crossword answer or clues for crossword answers. Here are the possible solutions for "Lower jaw" clue. Crouzon syndrome belongs to a large and heterogeneous group of conditions presenting with craniosynostosis, a common symptom of which is early fusion of one or more cranial sutures. 2. This can result in wide-set, bulging eyes. If you are currently working on a puzzle and find yourself in need of a little guidance, our answer is at your service. It occurs in one of every 25,000 births. G. , 2019). The cheeks and lower orbits are advanced. Sometimes surgery may be recommended as well. This crossword clue was last seen on 23 June 2023 in The Sun Coffee Time Crossword puzzle! Possible Answer. • It is the most common craniosynostosis syndrome. The Crossword Solver found 30 answers to "lower jaw (4)", 4 letters crossword clue. Activated FGFs/FGFR2 signaling disrupts the balance of differentiation, cell proliferation, and. useless. Sometimes surgery may be recommended as well. This syndrome results in wide-set, bulging eyes, an underdeveloped upper jaw, and a beaked nose due to the head being unable to grow normally. mutation in FGFR3 genes results in Crouzon syndrome with acanthosis nigricans. The Crossword Solver found 30 answers to "bird jaw (4)", 4 letters crossword clue. Severity of the syndrome varies from mild to severe among individuals. This surgery involves cutting and repositioning the upper jaw to improve how the jaws and the teeth fit together. This can result in prognathism or other head and facial irregularities. Small ears. Abstract. Approach Considerations. The disorder is characterized by distinctive malformations of the skull and facial (craniofacial) region. Prenatal diagnosis was performed on the high-risk f. Click the answer to find similar crossword clues . Sebenarnya tidak diketahui angka pasti dari kasus penyakit Gaucher ini. Many features of Crouzon syndrome result from the premature fusion of the skull bones. They allow the skull to expand as the child grows. We have the answer for Tip of lower jaw crossword clue in case you’ve been struggling to solve this one! Crosswords can be an excellent way to stimulate your brain, pass the time, and challenge yourself all at once. Blindness can occur if retinal detachments aren't. The developer, so-called Hitpas released many. 3. Crouzon Syndrome describes a combination of birth defects that occur as the result of a mutation of one of the genes at the time of conception. Crouzon's syndrome (CS) is a rare autosomal dominant condition with multiple mutations of the fibroblast growth factor receptor (FGFR2) gene. Today's crossword puzzle clue is a quick one: Lower jaw. Because, we know that if you finished this one, then the temptation to find the next puzzle is compelling. It involves the premature fusion of sutures of the cranial vault. It was first described by the French neurosurgeon Dr. Enter the length or pattern for better results. Click the answer to find similar crossword clues . In Crouzon syndrome, the bones in the skull and face. Differential diagnosis of Crouzon’s. Abnormal growth of these bones leads to wide-set, bulging eyes and vision problems caused by shallow eye sockets; eyes that do not point in the same direction (strabismus); a beaked nose; and an underdeveloped upper jaw. Enter the length or pattern for better results. Less common features of Crouzon syndrome with acanthosis nigricans include subtle changes in the bones of the spine (vertebrae), abnormalities of the finger bones, and noncancerous growths in the jaw called cementomas. Crouzon syndrome (CS) is an autosomal dominant genetic disorder characterized by craniofacial dysostosis. The prominent clinical features of the disease are (1) malformation of the cranium, that is, oxycephalia, in the area of the anterior fontanel and (2) under- development of the middle third of the face. Some people could develop it due to poor dental extractions. It can also be associated with Cleft lip and cleft palate. • Crouzon syndrome is estimated to affect about 1. Crouzon Syndrome is characterised by a premature fusing of certain skull bones during the fourth week of development; specifically affecting the lower jaw bone and the palate. Sort A-Z. Orthognathic surgery is the standard form of surgery to move either the upper or lower jaw into proper alignment. Enter the length or pattern for better results. Enter a Crossword Clue. Crouzon syndrome occurs in about one of every 100,000. Individuals with Crouzon syndrome usually have normal intelligence. Lower lip to E-line -1mm Y-axis to SN 64º Wits appraisal -6 Panoramic radiography ndings The patient’s upper third molars were missing congenitally. Levels of maternal somatic mosaicism for the mutation were estimated to range from 3. Johnson, MA; Publication Type: Condition. There are related clues (shown below). It can lead to enlarged tissues, such as an oversized jaw. charges (4) Crossword Clue. The triad composed by cranium deformities, facial anomalies and exophthalmia, described by Crouzon in 1912, forms today the Crouzon's syndrome (5,6,7,19). Crouzon syndrome was made on the basis of clinical, ocular, and radiological findings. The incidence of the disease significantly increases with paternal age and is felt to provide a selective advantage within the male spermatogonial cells. Enter the length or pattern for better results. The lack of hands and foot anomalies is crucial to distinguish Crouzon. It may develop over time in children or adults as the result of excess growth in conditions such as gigantism or acromegaly. 1 Craniosynostosis is the premature fusion of the skull bones. Help heal more kids. It is the most common form of craniosynostosis. g. com. In cases of craniofacial deformities, a specialist team will be needed for follow up and treatment. Lower Jaw Part. O. Clue Enter length and letters 2. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. A core category emerged labelled. The Crossword Solver found 30 answers to "point of the jaw (4)", 4 letters crossword clue. We presented a 6-year. [1,4] The. Here the authors described a Crouzon syndrome case, which was asked for surgery treatment for the symptom of multisuture. Bones in the face may also be fused together, resulting in a flat midface and protruding eyes. “Danner has always had horrible sleep apnea,” Sara explains. Michael We propose embryonic development of the lower jaw, including Meckel’s cartilage and mandibular bone, may be affected in Crouzon syndrome. Abstract. Learn about your child's treatment options at UPMC Children's Hospital . 42 The term “Crouzon syndrome” describes an autosomal disease, which results from hereditary mutations identified in specific genes in the human DNA chain. Not all answers shown, provide a pattern or longer clue for more results. cheekbones and upper jaw do not grow in proportion to the rest of the skull. 7 Crouzon patients (4 females, 3 males). It is a disorder caused by mutations in a specific gene — the fibroblast growth factor receptor 2 (FGFR2) gene. O. 6 in 100,000 people in the general population. In 1985, Dr. useless. Find the latest crossword clues from New York Times Crosswords, LA Times Crosswords and many more. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Flattered cheeks. Crouzon syndrome is a debilitating congenital disorder involving abnormal craniofacial skeletal development caused by mutations in fibroblast growth factor receptor-2 (FGFR2). Crouzon syndrome, also known as craniofacial dysostosis, is a complex genetic birth disorder that may affect a child’s face, skull, and teeth. A positive family history is reported to occur in 44-67% of cases. Enter the crossword clue and click "Find" to search for answers to crossword puzzle clues. Crouzon syndrome is a genetic congenital condition characterized by skeletal and facial malformations. Small and poorly formed upper jaw and a protruding lower jaw; Hearing loss; Cleft lip (opening in the lip). The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Crouzon syndrome affects 16 births out of 1 million. Here the authors described a Crouzon syndrome case, which was asked for surgery treatment for the symptom of multisuture. Answer of Figgerits Crouzon syndrome results in lower jaw __: PROTRUSION. Crouzon’s syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. It can also be caused by inherited conditions, such as Crouzon syndrome or basal cell nevus syndrome. It was last seen in The LA Times quick crossword. g. The Crossword Solver found 30 answers to "Jaw cheek (4)", 4 letters crossword clue. Crouzon syndrome is a genetic disorder that results in the bones of the face and skull joining in the wrong way. Some of the symptoms of Crouzon Syndrome are. Clue: Lower jaw. He had hydrocephalus since infancy and recently suffered from frequent dizziness. 7% and 5. Crouzon syndrome: (craniofacial dysostosis type 1 [CFD1]; Crouzon craniofacial dysostosis; Crouzon disease). Bulging, wide-set eyes. Search for crossword clues found in the Daily Celebrity, NY Times, Daily Mirror, Telegraph and major publications. Crouzon syndrome is a congenital condition that is diagnosed on the basis of a specific pattern of cranial and facial malformations. The clinical findings prompted a diagnosis of Crouzon syndrome. Crouzon syndrome is a genetic condition, caused by a mutation (change) on a specific gene. Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. In addition, affected individuals may also. The Crossword Solver finds answers to classic crosswords and cryptic crossword puzzles. Crouzon syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). In the 1990s, for example, they learned that a mutation in one gene causes Crouzon syndrome — characterized by wide-set, often bulging eyes and an underdeveloped upper jaw — while a mutation in a different gene leads to the down-slanting eyes, small lower jaw and cleft palate of Treacher Collins syndrome. Enter a Crossword Clue. Advice on follow-up and treatment. In children with a craniosynostosis syndrome, bones that fuse prematurely in the skull result in abnormal head shapes. The tongue often falls back in the throat, causing. 4. Patients report headache. Curved, beak-like nose. In permanent dentition, crown height, mesiodistal and faciolingual cervical diameters were reduced by 6. This can result in wide-set, bulging eyes. We showed that permanent but not primary tooth dimensions were globally reduced in Crouzon syndrome, without microdontia. Clue: Lower jaw. The palate is also very narrow. We report an 11 and a half-year-old boy with Crouzon syndrome with severe growth retardation. Moving of the bone of the upper and lower jaw to correct further irregularities in the bite. Enter the length or pattern for better results. Crouzon syndrome, also known as craniofacial dysostosis, is a complex genetic birth disorder that may affect a child’s face, skull, and teeth. The Crossword Solver found 30 answers to "protruding jaw part", 4 letters crossword clue. This term means that at least one of a person's skull bones fuses prematurely. Premature fusion of the skull bones prevents the skull from growing normally and affects the shape of the child’s head and face. Crouzon syndrome makes up approximately 4. Antley-Bixler Syndrome. Simak penjelasan selengkapnya mengenai gejala, penyebab, hingga cara. Enter the length or pattern for better results. Lower jaw Crossword Clue Answers. He described the triad of calvarial deformities, facial anomalies, and exophthalmos. Symptoms. Early fusion of the skull bones prevents the skull from. 5. All solutions for "lower jaw" 8 letters crossword answer - We have 2 clues, 5 answers & 3 synonyms from 4 to 8 letters. This syndrome has been associated with a variety of amino acid point mutations in the extracellular domain of fibroblast growth factor receptor 2. This condition is also known as craniosysnostosis. You may want to know the content of nearby topics so these links.