Hypochondroplasia with Acanthosis Nigricans and Moyamoya Disease-Reference-Cited by-同舟云学术

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Hypochondroplasia with Acanthosis Nigricans and Moyamoya Disease

Published:2023-04-01 Issue:2 Volume:31 Page:148-150
ISSN:2635-909X
Container-title:Annals of Child Neurology
language:en
Short-container-title:Ann Child Neurol

Author:

Lee Yoo Jung^ORCID,Jo Yoon Hee,Kim Mun-Bum,Kim Young Mi^ORCID

Funder

Pusan National University Hospital

Publisher

The Korean Child Neurology Society

Subject

Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Link

http://annchildneurol.org/upload/pdf/acn-2022-00402.pdf

Reference10 articles.

1. Acanthosis Nigricans: A practical approach to evaluation and management

2. Familial Acanthosis Nigricans Due to K650T FGFR3 Mutation

3. Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype

4. Acanthosis nigricans in a Chinese girl with FGFR3 K650 T mutation: a case report and literature review

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