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Clin Genet ; 92(5): 561-562, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28940199

ABSTRACT

Identification of this additional patient from a distant part of the originally described pedigree (Synofzik et al. 2014) confirms pathogenicity of DNAJC3 mutations. Hypothyroidism is a newly identified feature in addition to the known phenotype (diabetes with multisystemic neurodegeneration).


Subject(s)
Congenital Hypothyroidism/complications , Congenital Hypothyroidism/genetics , Diabetes Mellitus/genetics , HSP40 Heat-Shock Proteins/genetics , Mutation/genetics , Nerve Degeneration/complications , Nerve Degeneration/genetics , Female , Humans , Male , Pedigree , Phenotype , Young Adult
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