Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Brachydactyly type A3 is an autosomal dominant disorder which genetic background remains to be determined. Characteristic is a shortage or even absence of middle phalanges of the little digit. Patients exhibit a short stature and some other skeletal abnormalities.
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Williams KD et al. (2007) Heritability of brachydactyly type A3 in children, adolescents, and young adults from an endogamous population in eastern Nepal. 
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| 2. |
Buschang PH et al. (1980) Brachymesophalangia-V in five samples of children: a descriptive and methodological study.
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| 3. |
HERSH AH et al. (1953) On the inheritance and development of clinodactyly.
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None (1965) THE INHERITANCE OF THE RADIALLY CURVED LITTLE FINGER.
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| 5. |
OMIM.ORG article Omim 112700
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| 6. |
Wikipedia article Wikipedia EN (Brachydactyly)
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