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亚当斯-奥利弗综合征：一种罕见的先天性疾病。

Adams-Oliver Syndrome: A Rare Congenital Disorder.

作者信息

Rashid Sumara, Azeem Saleha, Riaz Samiha

机构信息

Dermatology, Fatima Memorial College of Medicine and Dentistry, Lahore, PAK.

Dermatology, King Edward Medical University, Lahore, PAK.

出版信息

Cureus. 2022 Mar 18;14(3):e23297. doi: 10.7759/cureus.23297. eCollection 2022 Mar.

DOI:10.7759/cureus.23297
PMID:35449659
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9012592/
Abstract

We present a case of a two-day-old Asian female infant with typical symptoms of Adams-Oliver syndrome (AOS): two cutaneous lesions including aplasia cutis congenita (ACC) and hypoplastic phalanges. The lesion on the abdomen is a relatively rare finding of the syndrome. Skin and skull bone were absent in the anterior fontanelle region, and hypertrophic labia minora was observed. The patient was put on regular follow-up.

摘要

我们报告一例两天大的亚洲女婴，患有亚当斯-奥利弗综合征（AOS）的典型症状：两处皮肤病变，包括先天性皮肤发育不全（ACC）和指骨发育不全。腹部的病变是该综合征相对罕见的表现。前囟区域皮肤和颅骨缺失，并观察到小阴唇肥大。该患者进行了定期随访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/1ba862d731fa/cureus-0014-00000023297-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/11a83610d106/cureus-0014-00000023297-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/c0f96da449d2/cureus-0014-00000023297-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/6ca31412b0ee/cureus-0014-00000023297-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/1ba862d731fa/cureus-0014-00000023297-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/11a83610d106/cureus-0014-00000023297-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/c0f96da449d2/cureus-0014-00000023297-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/6ca31412b0ee/cureus-0014-00000023297-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e9/9012592/1ba862d731fa/cureus-0014-00000023297-i04.jpg

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本文引用的文献

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2
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3
Dermatologic findings of focal dermal hypoplasia (Goltz syndrome).局灶性真皮发育不全（戈尔茨综合征）的皮肤表现。
Front Pediatr. 2025 Mar 3;13:1532561. doi: 10.3389/fped.2025.1532561. eCollection 2025.
4
Utilizing Spermatogenesis and Fertilization Mutants as a Model for Human Disease.利用精子发生和受精突变体作为人类疾病模型。
J Dev Biol. 2025 Jan 25;13(1):4. doi: 10.3390/jdb13010004.
Am J Med Genet C Semin Med Genet. 2016 Mar;172C(1):44-51. doi: 10.1002/ajmg.c.31472. Epub 2016 Feb 9.
4
Adams-Oliver syndrome.亚当斯-奥利弗综合征
J Coll Physicians Surg Pak. 2014 May;24 Suppl 2:S76-7.
5
Adams-Oliver Syndrome. A case with isolated aplasia cutis congenita and skeletal defects.亚当斯-奥利弗综合征。一例孤立性先天性皮肤发育不全伴骨骼缺陷的病例。
J Dermatol Case Rep. 2012 Mar 27;6(1):25-8. doi: 10.3315/jdcr.2012.1092.
6
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7
[Aplasia cutis congenita: surgical treatment and results in 36 cases].[先天性皮肤发育不全：36例手术治疗及结果]
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Autosomal dominant inheritance of scalp defects with ectrodactyly.
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