Recurrent Erythema Nodosum in a Child with a SHOC2 Gene Mutation

We report the case of a 6-year-old male who developed recurrent erythema nodosum (EN) at the age of 3 years. The patient exhibited hypertelorism, low-set ears, micrognathia, moderate intellectual disability, thin long fingers, loose anagen hair, and prominent palmoplantar wrinkles. A heterozygous si...

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Detaylı Bibliyografya
Yayımlandı:Yonago Acta Med
Asıl Yazarlar: Okazaki, Tetsuya, Saito, Yoshiaki, Sugita, Kazunari, Nosaka, Kanae, Ohno, Koyo, Hiraoka, Yumie, Kasagi, Noriko, Ebiki, Mitsutaka, Narai, Satoshi, Kawashima, Yuki, Takano, Shuichi, Kai, Masachika, Adachi, Kaori, Yamamoto, Osamu, Nanba, Eiji, Maegaki, Yoshihiro
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Tottori University Faculty of Medicine 2019
Konular:
Patient Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6437419/
https://ncbi.nlm.nih.gov/pubmed/30962759
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