Publication year
2001Source
Prenatal Diagnosis, 21, 13, (2001), pp. 1119-22ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
Nursing Home Medicine
Journal title
Prenatal Diagnosis
Volume
vol. 21
Issue
iss. 13
Page start
p. 1119
Page end
p. 22
Subject
Elucidation of hereditary disorders and their molecular diagnosis; Opheldering van erfelijke ziekten en hun moleculaire diagnostiekAbstract
We report the prenatal diagnosis at 16 weeks' gestation of bilateral split-hand/split-foot malformation (SHSFM) with severe lobster claw deformity of hands and feet in a male fetus without associated malformations. A minor manifestation of SHSFM was present in the father with only mild bilateral foot involvement (syndactyly I-II; cleft II-III; left cutaneous syndactyly III-IV). Mutation analysis of the p63 gene on chromosome 3q27 showed a missense mutation 577A-->G (predicting amino acid substitution K193E) in the father. This mutation has not been reported so far in SHSFM but resembles the previously reported 580A-->G (predicting amino acid substitution K194E) in a family with SHSFM.
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- Faculty of Medical Sciences [94202]
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