Pigmented hypertrichotic dermatosis: manifestations of a rare syndrome.
作者信息
Sialiti Sanae, Mansouri Siham, Khallaayoune Mehdi, Senouci Karima
机构信息
Department of Dermatology-Venereology, CHU Ibn Sina, Rabat, Morocco, Rabat, Morocco.
Department of Dermatology-Venereology, CHU Ibn Sina, Rabat, Morocco, Rabat, Morocco
出版信息
BMJ Case Rep. 2021 Apr 1;14(4):e241838. doi: 10.1136/bcr-2021-241838.
Abstract
摘要
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本文引用的文献
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A Turkish girl with H syndrome: stunted growth and development of autoimmune insulin dependent diabetes mellitus in the 6th year of diagnosis.一名患有H综合征的土耳其女孩：诊断后第6年出现生长发育迟缓及自身免疫性胰岛素依赖型糖尿病。
J Pediatr Endocrinol Metab. 2019 Jan 28;32(1):89-93. doi: 10.1515/jpem-2018-0380.
2
The H Syndrome: A Genodermatosis.H综合征：一种遗传性皮肤病。
Cureus. 2018 Jun 8;10(6):e2763. doi: 10.7759/cureus.2763.
3
H syndrome: the first 79 patients.H 综合征：79 例首诊患者
J Am Acad Dermatol. 2014 Jan;70(1):80-8. doi: 10.1016/j.jaad.2013.09.019. Epub 2013 Oct 27.
4
SLC29A3 mutation in a patient with syndromic diabetes with features of pigmented hypertrichotic dermatosis with insulin-dependent diabetes, H syndrome and Faisalabad histiocytosis.患者存在 SLC29A3 基因突变，表现为伴有胰岛素依赖型糖尿病、H 综合征和费萨拉巴德组织细胞增生症特征的综合征性糖尿病，伴有色素性多毛性角化过度皮肤病。
Diabetes Metab. 2013 May;39(3):281-5. doi: 10.1016/j.diabet.2013.03.007. Epub 2013 Apr 23.
5
The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations.H综合征：一种遗传性皮肤病，其特征为皮肤硬结、色素沉着和多毛，并伴有全身表现。
J Am Acad Dermatol. 2008 Jul;59(1):79-85. doi: 10.1016/j.jaad.2008.03.021. Epub 2008 Apr 14.
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