Format

Send to

Choose Destination
See comment in PubMed Commons below
Ann Pediatr (Paris). 1991 Jan;38(1):31-6.

[Acrodysostosis in a sister and brother born to normal parents].

[Article in French]

Author information

  • 1URA 584 du CNRS, Clinique Maurice Lamy, Hôpital des Enfants-Malades, Paris.

Abstract

Two cases of acrodysostosis syndrome in a brother and sister are reported. The parents and other siblings were unaffected. Features of this syndrome include extremely short, broad metacarpals, metatarsals, and phalanges, nasal hypoplasia, short stature, and mental deficiency. Previously published familial cases of acrodysostosis syndrome are consistent with autosomal dominant transmission, whereas the cases reported herein suggest other genetic mechanisms including recessive autosomal transmission, unstable mutation, and germ cell mosaicism, the latter being the most attractive hypothesis.

PMID:
2006831
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Loading ...
    Write to the Help Desk