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Fountain syndrome - Wikipedia, the free encyclopedia

Fountain syndrome

From Wikipedia, the free encyclopedia

Fountain syndrome
Classification and external resources
OMIM 229120

Fountain syndrome is an autosomal recessive congenital disorder characterized by mental retardation, deafness, skeletal abnormalities and a coarse face with full lips.

Fountain syndrome has an autosomal recessive pattern of inheritance.
Fountain syndrome has an autosomal recessive pattern of inheritance.

[edit] References

  • Fountain RB (1974). "Familial bone abnormalities, deaf mutism, mental retardation and skin granuloma". Proc R Soc Med 67 (9): 878-879. PMID 4431800. 
  • Fryns JP (1989). "Fountain's syndrome: mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips". J Med Genet 26 (11): 722-724. PMID 2585470. 
  • Fryns JP, Dereymaeker A, Hoefnagels M, Van den Berghe H (1987). "Mental retardation, deafness, skeletal abnormalities, and coarse face with full lips: confirmation of the Fountain syndrome". Am J Med Genet 26 (3): 551-555. doi:10.1002/ajmg.1320260307. PMID 3565469. 

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