Literature DB >> 11422978

Prenatal diagnosis of type A1 brachydactyly.

N S den Hollander1, A J Hoogeboom, M F Niermeijer, J W Wladimiroff.   

Abstract

Brachydactyly can occur as an isolated malformation or as part of numerous syndromes. Prenatal assessment of brachydactyly may be especially helpful in multiple anomaly syndromes associated with hand and/or finger anomalies. In isolated type A1 brachydactyly, which is an autosomal dominant disorder, all middle phalanges of the fingers and toes are affected. We present a fetus with type A1 brachydactyly inherited from the mother and grandmother.

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Year:  2001        PMID: 11422978     DOI: 10.1046/j.1469-0705.2001.00428.x

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  2 in total

1.  A 6.3 Mb maternally derived microduplication of 20p13p12.2 in a fetus with Brachydactyly type D and related literature review.

Authors:  Guangquan Chen; Shiyi Xiong; Gang Zou; Fengyu Wu; Xiaoxing Qu; Salem Alawbathani; Luming Sun
Journal:  Mol Cytogenet       Date:  2022-02-28       Impact factor: 2.009

2.  A new biometric: In utero growth curves for metacarpal and phalangeal lengths reveal an embryonic patterning ratio.

Authors:  Rashmi Rao; Jeffrey Gornbein; Yalda Afshar; Lawrence D Platt; Greggory R DeVore; Deborah Krakow
Journal:  Prenat Diagn       Date:  2019-02-11       Impact factor: 3.050

  2 in total

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