Kaufman oculocerebrofacial syndrome

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Kaufman oculocerebrofacial syndrome
Classification and external resources
OMIM 244450

Kaufman oculocerebrofacial syndrome is an autosomal recessive congenital disorder characterized by mental retardation, microbrachycephaly, long narrow face, upslanting palpebral fissures, eye abnormalities, highly arched palate, preauricular skin tags and small mandible.

Kaufman oculocerebrofacial syndrome has an autosomal recessive pattern of inheritance.
Kaufman oculocerebrofacial syndrome has an autosomal recessive pattern of inheritance.

[edit] References

  • Kaufman R, Rimoin D, Prensky A, Sly W (1971). "An oculocerebrofacial syndrome.". Birth Defects Orig Artic Ser 7 (1): 135-138. PMID 5006210. 
  • Jurenka S, Evans J (1979). "Kaufman oculocerebrofacial syndrome: case report.". Am J Med Genet 3 (1): 15-19. doi:10.1002/ajmg.1320030106. PMID 112864. 
  • Figuera L, García-Cruz D, Ramírez-Dueñas M, Rivera-Robles V, Cantù J (1993). "Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation.". Clin Genet 44 (2): 98-101. PMID 8275567. 
  • Briscioli V, Manoukian S, Selicorni A, Livini E, Lalatta F (1995). "Kaufman oculocerebrofacial syndrome in a girl of 15 years.". Am J Med Genet 58 (1): 21-13. doi:10.1002/ajmg.1320580106. PMID 7573151. 
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