A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities - PubMed (original) (raw)
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A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities
J Elliott et al. J Med Genet. 1993 Mar.
Abstract
An interstitial deletion of the region q22.1-->q22.3 of chromosome 14 is described in a child with bilateral anophthalmia, dysmorphic features including micrognathia, small tongue, and high arched palate, developmental and growth retardation, undescended testes with a micropenis, and hypothyroidism. Interstitial deletions of the long arm of chromosome 14 are extremely rare, but this case seems to confirm that the region q22 is specifically concerned with pituitary and eye development.
References
- J Med Genet. 1978 Jun;15(3):236-8 - PubMed
- J Med Genet. 1983 Apr;20(2):147-9 - PubMed
- Ann Genet. 1984;27(4):237-40 - PubMed
- J Med Genet. 1991 Apr;28(4):280-1 - PubMed
- J Med Genet. 1989 Feb;26(2):130-3 - PubMed
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