一名糖尿病患者出现色素沉着过度斑块伴多毛症。 - Suppr

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Hyperpigmented plaques with hypertrichosis in a patient with diabetes mellitus.

作者信息

Perea Polak Alexandra, Romero Madrid Beatriz, Vera Casaño Angel, Andamoyo Castañeda Alberto, Gomez Moyano Elizabeth

机构信息

Department of Dermatology, Hospital Regional Universitario de Málaga, Malaga, Spain.

Department of Pathology, Hospital Regional Universitario de Málaga, Malaga, Spain.

出版信息

Pediatr Dermatol. 2021 Jan;38(1):269-271. doi: 10.1111/pde.14400.

DOI:10.1111/pde.14400

PMID:33630370

Abstract

摘要

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Hyperpigmented plaques with hypertrichosis in a patient with diabetes mellitus.

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Hyperpigmented plaques with hypertrichosis in a patient with diabetes mellitus.

作者信息

Perea Polak Alexandra, Romero Madrid Beatriz, Vera Casaño Angel, Andamoyo Castañeda Alberto, Gomez Moyano Elizabeth

机构信息

Department of Dermatology, Hospital Regional Universitario de Málaga, Malaga, Spain.

Department of Pathology, Hospital Regional Universitario de Málaga, Malaga, Spain.

出版信息

Pediatr Dermatol. 2021 Jan;38(1):269-271. doi: 10.1111/pde.14400.

DOI:10.1111/pde.14400

PMID:33630370

Abstract

摘要

相似文献

Hyperpigmented plaques with hypertrichosis in a patient with diabetes mellitus.

Pediatr Dermatol. 2021 Jan;38(1):269-271. doi: 10.1111/pde.14400.

Mutation in the SLC29A3 gene: a new cause of a monogenic, autoinflammatory condition.

Pediatrics. 2013 Apr;131(4):e1308-13. doi: 10.1542/peds.2012-2255. Epub 2013 Mar 25.

A novel 3' untranslated region mutation in the SLC29A3 gene associated with pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus syndrome.

Pediatr Diabetes. 2019 Jun;20(4):474-481. doi: 10.1111/pedi.12839. Epub 2019 Apr 2.

[H syndrome: First reported paediatric case in Latin America].

Rev Chil Pediatr. 2016 Nov-Dec;87(6):494-499. doi: 10.1016/j.rchipe.2016.03.006. Epub 2016 Apr 30.

The H syndrome is caused by mutations in the nucleoside transporter hENT3.

Am J Hum Genet. 2008 Oct;83(4):529-34. doi: 10.1016/j.ajhg.2008.09.013.

Clinical, Histochemical, and Molecular Study of Three Turkish Siblings Diagnosed with H Syndrome, and Literature Review.

Horm Res Paediatr. 2019;91(5):346-355. doi: 10.1159/000495190. Epub 2019 Jan 9.

Identification of a novel homozygous frameshift mutation in SLC29A3 gene in a case with H syndrome from Iran.

Curr Res Transl Med. 2019 May;67(2):72-75. doi: 10.1016/j.retram.2019.01.003. Epub 2019 Feb 2.

Cases with the H syndrome presenting with skin and bone findings.

Australas J Dermatol. 2024 Jun;65(4):337-341. doi: 10.1111/ajd.14235. Epub 2024 Feb 29.

H syndrome: the first 79 patients.

J Am Acad Dermatol. 2014 Jan;70(1):80-8. doi: 10.1016/j.jaad.2013.09.019. Epub 2013 Oct 27.

Hyperpigmented and hypertrichotic sclerotic plaques in a child.

Pediatr Dermatol. 2020 Sep;37(5):937-938. doi: 10.1111/pde.14258.