Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2000 Apr;37(4):292-6.
doi: 10.1136/jmg.37.4.292.

Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profiles

Affiliations
Case Reports

Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profiles

C M Armour et al. J Med Genet. 2000 Apr.

Abstract

The brachydactylies are a group of conditions in which various subtypes have been defined based upon the specific pattern of digital bones involved. Type A1 brachydactyly is principally characterised by maximal involvement of the middle phalanges. We report an extended family with a mild brachydactyly A1 which was, except for some short stature, not associated with any of the additional clinical findings reported in several published families. While all the hand bones tended to be small, the principal features of the affected members were shortened middle and distal phalanges, proximal 1st phalanges, and 5th metacarpals. The feet were similarly involved and tended to have a broad, slightly adducted forefoot. The two affected children showed multiple coned epiphyses. This paper provides a detailed description of the family including the radiographic signs and metacarpophalangeal profiles, which proved to be useful in distinguishing the mildly affected persons.

PubMed Disclaimer

References

    1. Radiology. 1972 Jul;104(1):1-11 - PubMed
    1. Radiology. 1972 Nov;105(2):375-81 - PubMed
    1. J Med Genet. 1979 Feb;16(1):36-44 - PubMed
    1. Clin Dysmorphol. 1998 Jan;7(1):29-34 - PubMed
    1. Am J Med Genet. 1995 Jul 3;57(3):447-9 - PubMed

Publication types