#123500 ICD+
  • ICD10CM: Q75.1,
  • SNOMEDCT: 28861008
ICD10CM: Q75.1, SNOMEDCT: 28861008
CROUZON SYNDROME

Alternative titles; symbols
CRANIOFACIAL DYSOSTOSIS, TYPE I; CFD1
CROUZON CRANIOFACIAL DYSOSTOSIS

Phenotype Gene Relationships
Location Phenotype Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
10q26.13 Crouzon syndrome 123500 FGFR2 176943


TEXT
A number sign (#) is used with this entry because of evidence that Crouzon syndrome is caused by mutation in the gene encoding fibroblast growth factor receptor-2 (FGFR2; 176943).

See also Crouzon syndrome with acanthosis nigricans (CAN; 612247), a distinct disorder caused by a specific mutation in the FGFR3 gene (A391E; 134934.0011).

Description
Crouzon syndrome is an autosomal dominant disorder characterized by craniosynostosis causing secondary alterations of the facial bones and facial structure. Common features include hypertelorism, exophthalmos and external strabismus, parrot-beaked nose, short upper lip, hypoplastic maxilla, and a relative mandibular prognathism (Reardon et al., 1994; Glaser et al., 2000).

Clinical Features
Crouzon (1912) first described this syndrome in a family.

Shiller (1959) observed autosomal dominant transmission of Crouzon craniofacial dysostosis in 23 family members spanning 4 generations. There was marked variability in both cranial and facial manifestations. Dodge et al. (1959) described 3 patients with typical Crouzon disease; 2 of these had a positive family history and one was sporadic.

Devine et al. (1984) described a completely cartilaginous trachea without ring formation in a child with Crouzon syndrome who continued to have respiratory distress despite surgical repair of choanal stenosis. Death from respiratory problems occurred at the age of 23 months.

Cohen et al. (1993) reported a mother, son, and daughter in whom serial photographs documented an insidious and late onset of exorbitism and midfacial retrusion. Papilledema resulting from increased intracranial pressure secondary to a reduction in cranial vault size was found in the 4.5-year-old daughter, whereas optic nerve sheath swelling was found on CT scan in the son.

Reddy et al. (1990) described 4 patients who presented between the ages of 2 and 9 years with 'delayed holocalvarial synostosis.'

Cinalli et al. (1995) reviewed the neurosurgical complications of Crouzon syndrome in a series of 68 patients. Nineteen of these patients required treatment for progressive hydrocephalus and 72.7% of these patients had chronic tonsillar herniation, which was symptomatic in 6 individuals. Four individuals had syringomyelia and another had a respiratory standstill, whereas the remaining patient had painful torticollis.

Inheritance
Fogh-Andersen (1943), Flippen (1950), and Shiller (1959) traced Crouzon craniosynosostosis through 4 generations of 3 different families, consistent with autosomal dominant inheritance. Pinkerton and Pinkerton (1952) observed the disorder in a mother and 2 of her 3 daughters.

Vulliamy and Normandale (1966) identified 14 cases of Crouzon disease in 4 generations of a family with several instances of male-to-male transmission.

Jones et al. (1975) found evidence of paternal age effect in new mutations for this disorder.

Rollnick (1988) described 2 brothers with Crouzon syndrome born to normal, unrelated parents, and proposed germinal mosaicism as the explanation. Kreiborg and Cohen (1990) suggested germinal mosaicism as the basis for 2 affected sibs with the same mother but different fathers. The mother and both fathers were completely normal.

Goriely et al. (2010) reported a girl with a mild form of Crouzon syndrome, confirmed by genetic analysis, whose clinically unaffected mother was found to be somatic mosaic for a heterozygous FGFR2 mutation. Levels of maternal somatic mosaicism for the mutation were estimated to range from 3.3% in hair roots to 14.1% in blood. Since her daughter inherited the same mutation, it was presumed to be present also in the mother's germline. The findings underlined the importance of parental molecular testing for accurate genetic counseling of the risk of recurrence for Crouzon syndrome, which is most often due to a de novo mutation resulting from a paternal age effect.

Mapping
In a large kindred with Crouzon craniofacial dysostosis, Preston et al. (1994) found linkage to 3 loci (D10S190, D10S209, and D10S216) spanning a 13-cM region on chromosome 10q. A maximum pairwise lod score of 4.42 at theta = 0.0 was obtained with D10S190 and the addition of a second kindred produced a combined pairwise lod score of 5.32 at theta = 0.0. In a note added in proof, Preston et al. (1994) stated that a newly available highly informative marker, D10S587, located 7 cM distal to D10S209, increased the 2-family multipoint lod score for linkage between CFD1 and D10S209 to 7.3 at theta = 0.0. Two of the genetic marker loci were within 10q25-q26.

Molecular Genetics
Reardon et al. (1994) identified mutations in the FGFR2 gene (see, e.g., 176943.0001-176943.0006) in 9 of 20 patients with Crouzon syndrome. Because no evidence of genetic heterogeneity on the basis of linkage studies had been found, Reardon et al. (1994) concluded that mutations in parts of the FGFR2 gene other than in the B exon were responsible for the remaining cases.

Jabs et al. (1994) demonstrated mutations in the FGFR2 gene in patients with Crouzon syndrome as well as in patients with Jackson-Weiss syndrome (JWS; 123150).

Charnas et al. (1989) described affected male and female second cousins, and suggested either incomplete penetrance or another molecular predisposition ('premutation'). However, Meyers et al. (1995) reported that the 2 patients described by Charnas et al. (1989) had mutations in different genes: the patient with classic Crouzon syndrome had an FGFR2 mutation (176943.0009), whereas the second cousin had Crouzon syndrome with acanthosis nigricans (612247) due to the FGFR3 A391E mutation (134934.0001).

In 22 of 41 probands with Crouzon syndrome or Pfeiffer syndrome (101600), Glaser et al. (2000) identified 11 different FGFR2 mutations. All the mutations were paternal in origin. Advanced paternal age was noted for the fathers of patients with Crouzon syndrome or Pfeiffer syndrome, compared with the fathers of control individuals. This finding extended previous information on advanced paternal age for sporadic FGFR2 mutations causing Apert syndrome (101200) and FGFR3 mutations causing achondroplasia (100800).

Population Genetics
Cohen and Kreiborg (1992) estimated that Crouzon syndrome represents approximately 4.8% of cases of craniosynostosis at birth. The birth prevalence was estimated to be 16.5 per million births.

History
On the basis of an affected brother and sister with unaffected nonconsanguineous parents, Juberg and Chambers (1973) suggested the existence of a recessive form of Crouzon disease.

Pseudo-Crouzon Syndrome

Franceschetti (1953) described a seemingly distinct disorder under the designation cranial dysostosis with pronounced digital impressions, or 'pseudo-Crouzon disease.' However, Gorlin (1982) concluded that it is not distinct from Crouzon disease. According to Franceschetti's appraisal, in Crouzon disease and pseudo-Crouzon disease, the pronounced digital impressions, or convolutional markings, are identical, and the essential difference is in the face: in pseudo-Crouzon disease, there is no prognathism, the nose is not curved, and divergent squint is usually lacking. Prominent forehead and some degree of exophthalmos are features. Franceschetti (1968) proposed that Walsh (1957) described a case of pseudo-Crouzon disease as Crouzon disease. None of Franceschetti's cases was familial, but Dolivo and Gillieron (1955) described affected brother and sister whose mother, grandmother, and great-grandmother were said to have oxycephaly.

Animal Model
Eswarakumar et al. (2006) generated mice with a Crouzon-like craniosynostosis induced by a dominant mutation in the mesenchymal splice form of Fgfr2 (Fgfr2c) (C342Y; 176943.0001), and observed ocular proptosis, a rounded cranium, fusion of the coronal sutures, and a significantly shortened facial region. Expression of the C342Y mutation in cis with the L424A and R426A mutations of the juxtamembrane domain resulted in attenuation of signaling pathways by selective uncoupling between the docking protein Frs2a (607743) and activated Fgfr2c, thus preventing premature fusion of sutures and resulting in normal skull development. Eswarakumar et al. (2006) also demonstrated that attenuation of Fgfr signaling in a calvaria organ culture with an Fgfr inhibitor prevented premature fusion of sutures without adversely affecting the development of the skull.

See Also:
Kreiborg and Jensen (1977)

REFERENCES
1. Charnas, L., Hofman, K. J., Rosenbaum, K. N. Crouzon syndrome: evidence of incomplete penetrance (Abstract) Am. J. Hum. Genet. 45 (suppl.): A43, 1989.

2. Cinalli, G., Renier, D., Sebag, G., Sainte-Rose, C., Arnaud, E., Pierre-Kahn, A. Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture. J. Neurosurg. 83: 575-582, 1995. [PubMed: 7674004, related citations] [Full Text: Atypon, Pubget]

3. Cohen, M. M., Jr., Kreiborg, S. Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods. Clin. Genet. 41: 12-15, 1992. [PubMed: 1633640, related citations] [Full Text: Pubget]

4. Cohen, S. R., Dauser, R. C., Gorski, J. L. Insidious onset of familial craniosynostosis. Cleft-Palate Craniofac. J. 30: 401-405, 1993. [PubMed: 8399270, related citations] [Full Text: Pubget]

5. Crouzon, O. Dysostose cranio-faciale hereditaire. Bull. Mem. Soc. Med. Hop. Paris 33: 545-555, 1912.

6. Devine, P., Bhan, M., Feingold, M., Leonidas, J., Wolpert, S. Completely cartilaginous trachea in a child with Crouzon syndrome. Am. J. Dis. Child. 138: 40-43, 1984. [PubMed: 6546324, related citations] [Full Text: HighWire Press, Pubget]

7. Dodge, H. W., Wood, M. W., Kennedy, R. L. J. Craniofacial dysostosis: Crouzon's disease. Pediatrics 23: 98-106, 1959. [PubMed: 13613870, related citations] [Full Text: Pubget]

8. Dolivo, G., Gillieron, J.-D. Une famille de pseudo-Crouzon. Confin. Neurol. 15: 114-118, 1955. [PubMed: 14390947, related citations] [Full Text: Pubget]

9. Eswarakumar, V. P., Ozcan, F., Lew, E. D., Bae, J. H., Tome, F., Booth, C. J., Adams, D. J., Lax, I., Schlessinger, J. Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis. Proc. Nat. Acad. Sci. 103: 18603-18608, 2006. [PubMed: 17132737, related citations] [Full Text: HighWire Press, Pubget]

10. Flippen, J. H., Jr. Cranio-facial dysostosis of Crouzon: report of a case in which the malformation occurred in four generations. Pediatrics 5: 90-96, 1950. [PubMed: 15404650, related citations] [Full Text: Pubget]

11. Fogh-Andersen, P. Craniofacial dysostosis (Crouzon's disease) as a dominant hereditary affection. Nord. Med. 18: 993-996, 1943.

12. Franceschetti, A. Cranial dysostosis with pronounced digital impressions (pseudo-Crouzon dysostosis).In: Beard, C. : Congenital Anomalies of the Eye. St. Louis: C. V. Mosby (pub.) 1968. Pp. 81-84.

13. Franceschetti, A. Dysostose cranienne avec calotte cerebriforme (pseudo-Crouzon). Confin. Neurol. 13: 161-166, 1953. [PubMed: 13082990, related citations] [Full Text: Pubget]

14. Glaser, R. L., Jiang, W., Boyadjiev, S. A., Tran, A. K., Zachary, A. A., Van Maldergem, L., Johnson, D., Walsh, S., Oldridge, M., Wall, S. A., Wilkie, A. O. M., Jabs, E. W. Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome. Am. J. Hum. Genet. 66: 768-777, 2000. [PubMed: 10712195, related citations] [Full Text: Elsevier Science, Pubget]

15. Goriely, A., Lord, H., Lim, J., Johnson, D., Lester, T., Firth, H. V., Wilkie, A. O. M. Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: implications for genetic testing in 'paternal age-effect' syndromes. Am. J. Med. Genet. 152A: 2067-2073, 2010. [PubMed: 20635358, related citations] [Full Text: John Wiley & Sons, Inc., Pubget]

16. Gorlin, R. J. Personal Communication. Minneapolis, Minn. 1982.

17. Jabs, E. W., Li, X., Scott, A. F., Meyers, G., Chen, W., Eccles, M., Mao, J., Charnas, L. R., Jackson, C. E., Jaye, M. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nature Genet. 8: 275-279, 1994. [PubMed: 7874170, related citations] [Full Text: Nature Publishing Group, Pubget]

18. Jones, K. L., Smith, D. W., Harvey, M. A. S., Hall, B. D., Quan, L. Older paternal age and fresh gene mutation: data on additional disorders. J. Pediat. 86: 84-88, 1975. [PubMed: 1110452, related citations] [Full Text: Pubget]

19. Juberg, R. C., Chambers, S. R. An autosomal recessive form of craniofacial dysostosis (the Crouzon syndrome). J. Med. Genet. 10: 89-93, 1973. [PubMed: 4697859, related citations] [Full Text: HighWire Press, Pubget]

20. Kreiborg, S., Cohen, M. M., Jr. Germinal mosaicism in Crouzon syndrome. Hum. Genet. 84: 487-488, 1990. [PubMed: 2323783, related citations] [Full Text: Pubget]

21. Kreiborg, S., Jensen, B. L. Variable expressivity of Crouzon's syndrome within a family. Scand. J. Dent. Res. 85: 175-184, 1977. [PubMed: 265609, related citations] [Full Text: Pubget]

22. Meyers, G. A., Orlow, S. J., Munro, I. R., Przylepa, K. A., Jabs, E. W. Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. Nature Genet. 11: 462-464, 1995. [PubMed: 7493034, related citations] [Full Text: Nature Publishing Group, Pubget]

23. Pinkerton, O. D., Pinkerton, F. J. Hereditary craniofacial dysplasia. Am. J. Ophthal. 35: 500-506, 1952. [PubMed: 14914838, related citations] [Full Text: Pubget]

24. Preston, R. A., Post, J. C., Keats, B. J. B., Aston, C. E., Ferrell, R. E., Priest, J., Nouri, N., Losken, H. W., Morris, C. A., Hurtt, M. R., Mulvihill, J. J., Ehrlich, G. D. A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10. Nature Genet. 7: 149-153, 1994. [PubMed: 7920632, related citations] [Full Text: Nature Publishing Group, Pubget]

25. Reardon, W., Winter, R. M., Rutland, P., Pulleyn, L. J., Jones, B. M., Malcolm, S. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nature Genet. 8: 98-103, 1994. [PubMed: 7987400, related citations] [Full Text: Nature Publishing Group, Pubget]

26. Reddy, K., Hoffman, H., Armstrong, D. Delayed and progressive multiple suture craniosynostosis. Neurosurgery 26: 442-448, 1990. [PubMed: 2320213, related citations] [Full Text: Pubget]

27. Rollnick, B. R. Germinal mosaicism in Crouzon syndrome. Clin. Genet. 33: 145-150, 1988. [PubMed: 3359675, related citations] [Full Text: Pubget]

28. Shiller, J. G. Craniofacial dysostosis of Crouzon: a case report and pedigree with emphasis on heredity. Pediatrics 23: 107-112, 1959. [PubMed: 13613871, related citations] [Full Text: Pubget]

29. Vulliamy, D. G., Normandale, P. A. Cranio-facial dysostosis in a Dorset family. Arch. Dis. Child. 41: 375-382, 1966. [PubMed: 21032436, related citations] [Full Text: Pubget]

30. Walsh, F. B. Clinical Neuro-ophthalmology. Baltimore: Williams and Wilkins (pub.) (2nd ed.) : 1957.

Contributors: Cassandra L. Kniffin - updated : 1/11/2011
Cassandra L. Kniffin - reorganized : 9/4/2008
Marla J. F. O'Neill - updated : 4/17/2007
Orest Hurko - updated : 4/1/1996
Creation Date: Victor A. McKusick : 6/23/1986
Edit History: wwang : 01/31/2011
ckniffin : 1/11/2011
carol : 5/19/2010
carol : 3/15/2010
carol : 9/4/2008
ckniffin : 8/22/2008
wwang : 4/17/2007
mcapotos : 5/4/2000
mcapotos : 5/4/2000
carol : 12/6/1999
carol : 7/1/1998
terry : 6/19/1998
jenny : 10/21/1997
alopez : 7/7/1997
mark : 6/9/1997
terry : 4/1/1997
terry : 5/6/1996
terry : 4/15/1996
terry : 4/1/1996
terry : 3/22/1996
mark : 12/6/1995
carol : 1/23/1995
pfoster : 8/18/1994
davew : 7/28/1994
mimadm : 6/25/1994
jason : 6/15/1994
warfield : 4/8/1994