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・ Infantile acropustulosis
・ Infantile apnea
・ Infantile convulsions and choreoathetosis
・ Infantile cortical hyperostosis
・ Infantile digital fibromatosis
・ Infantile esotropia
・ Infantile fibromatosis
・ Infantile free sialic acid storage disease
・ Infantile hemangiopericytoma
・ Infantile myofibromatosis
・ Infantile neuroaxonal dystrophy
・ Infantile neuronal ceroid lipofuscinosis
・ Infantile progressive bulbar palsy
・ Infantile Refsum disease
・ Infantile speech
Infantile systemic hyalinosis
・ Infantilism
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Infantile systemic hyalinosis : ウィキペディア英語版
Infantile systemic hyalinosis

Infantile systemic hyalinosis or juvenile systemic hyalinosis is an allelic autosomal-recessive condition characterized by multiple skin nodules, hyaline deposition, gingival hypertrophy, osteolytic bone lesions, and joint contractures.〔James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.〕
==Genetics==

This disease is caused by mutations in the CMG2 gene.〔Vahidnezhad H, Ziaee V, Youssefian L, Li Q, Sotoudeh S, Uitto J (2015) Infantile systemic hyalinosis in an Iranian family with a mutation in the CMG2/ANTXR2 gene. Clin Exp Dermatol doi: 10.1111/ced.12616〕

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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