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仅累及上肢或仅累及下肢的先天性肌发育不全及相关鉴别诊断综述

Amyoplasia involving only the upper limbs or only involving the lower limbs with review of the relevant differential diagnoses.

作者信息

Hall Judith G

机构信息

Departments of Medical Genetics and Pediatrics, University of British Columbia, BC Children's Hospital Vancouver, British Columbia, Canada.

出版信息

Am J Med Genet A. 2014 Apr;164A(4):859-73. doi: 10.1002/ajmg.a.36397. Epub 2014 Jan 23.

DOI:10.1002/ajmg.a.36397
PMID:24459095
Abstract

Of individuals with Amyoplasia, 16.8% (94/560) involve only the upper limbs (Upper Limb Amyoplasia-ULA) and 15.2% (85/560) involve only the lower limbs (Lower Limb Amyoplasia-LLA). The accompanying paper deals with other forms of Amyoplasia [Hall et al., 2013] and discusses etiology. An excess of one of monozygotic (MZ) twins is seen in both groups (ULA 4/94 (4.3%), LLA 5/85 (5.9%)), gastrointestinal (GI) abnormalities thought to be of vascular origin (bowel atresia and gastroschisis) (ULA 16/94 (17%), LLA 4/85 (4.7%)), small or partial absence of digits (ULA 6/94 (6.2%), LLA 8/85 (9.4%)), and umbilical cord wrapping around the limbs at birth (ULA 3/94 (3.2%), LLA 7/85 (8.2%)) (severe enough to leave a permanent groove). Pregnancy complications occurred in 42/60 (70%) of ULA and 36/54 (67%) of LLA. Prenatal diagnosis, after ultrasound usage became routine, occurred in only 7/25 (28%) of ULA and 5/12 (12%) of LLA. This series may represent an over estimate of the complications and associations occurring in ULA and LLA. Differential diagnoses separating LLA from the genetic forms of "lower limb only" arthrogryposis and ULA from "upper limb only" genetic forms of arthrogryposis and Erb's palsy is provided.

摘要

在患有先天性肌发育不全的个体中,16.8%(94/560)仅累及上肢(上肢先天性肌发育不全-ULA),15.2%(85/560)仅累及下肢(下肢先天性肌发育不全-LLA)。随附论文讨论了先天性肌发育不全的其他形式[Hall等人,2013]并探讨了病因。在两组中都观察到单卵(MZ)双胞胎中的一方患病(ULA组4/94(4.3%),LLA组5/85(5.9%))、被认为是血管源性的胃肠道(GI)异常(肠闭锁和腹裂)(ULA组16/94(17%),LLA组4/85(4.7%))、手指短小或部分缺失(ULA组6/94(6.2%),LLA组8/85(9.4%))以及出生时脐带缠绕肢体(ULA组3/94(3.2%),LLA组7/85(8.2%))(严重到留下永久性凹槽)。42/60(70%) 的ULA患者和36/54(67%)的LLA患者出现妊娠并发症。在超声检查成为常规检查后,仅7/25(28%)的ULA患者和5/12(12%)的LLA患者进行了产前诊断。本系列可能高估了ULA和LLA中出现的并发症及关联情况。本文提供了将LLA与“仅累及下肢”的遗传性关节挛缩症以及将ULA与“仅累及上肢”的遗传性关节挛缩症和臂丛神经麻痹相鉴别的诊断方法。

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Response to Hall et al.对霍尔等人的回应
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Using the Term Amyoplasia Loosely Can Lead to Confusion.随意使用“无肌肉发育不良”这一术语可能会导致混淆。
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Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal Arthrogryposis.MYLPF 基因突变导致一种新型节段性肌无力,表现为远端关节挛缩。
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