<scp>Schimmelpenning–Feuerstein–Mims</scp> syndrome: A case series and brief literature review of genetically ascertained cases-Reference-Cited by-同舟云学术

Schimmelpenning–Feuerstein–Mims syndrome: A case series and brief literature review of genetically ascertained cases

Published:2022-11-21 Issue:3 Volume:37 Page:
ISSN:0926-9959
Container-title:Journal of the European Academy of Dermatology and Venereology
language:en
Short-container-title:Acad Dermatol Venereol

Author:

Miao Chaoyang¹^ORCID,He Rui¹,Yang Siyan²,Zhang Bin¹²^ORCID

Affiliation:

1. Department of Dermatology, Beijing Children's Hospital Capital Medical University (National Center for Children's Health, China) Beijing China

2. Department of Dermatology, Zhengzhou University, Affiliated Children's Hospital, Henan Children's Hospital Zhengzhou Children's Hospital Zhengzhou Henan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jdv.18749

Reference10 articles.

1. Choroid Osteoma in Schimmelpenning-Feuerstein-Mims Syndrome

2. The group of epidermal nevus syndromes

3. Schimmelpenning Syndrome: A Case Report and Literature Review

4. Didymosis aplasticosebacea: Coexistence of Aplasia cutis congenita and Nevus sebaceus May Be Explained as a Twin Spot Phenomenon

5. A postzygotic KRAS mutation in a patient with Schimmelpenning syndrome presenting with lipomatosis, renovascular hypertension, and diabetes mellitus

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