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Summary
ZINC DEFICIENCY, TRANSIENT NEONATAL TNZD
ZINC DEFICIENCY, NEONATAL, DUE TO LOW BREAST MILK ZINC
608118
OMIM = Online Medalian Inheritance of Men
1p36.11
very rare
autosomal dominant
maternal heterozygous mutation in the SLC30A2 gene
Symptoms occur only in exclusively breastfed infants
symptoms
alopecia
dermatitis
onset, infancy
laboratory finding
Zinc decreasedmothers breast milk
Zinc amniotic fluid
Literature
Khan SA,Shagufta KA rare case of fish odor syndrome presenting as depressionIndian J Psychiatry562185-1872014
DAngelo R,et al.Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case reportJ Med Case Rep803282014
Shimizu M,et al.Relationships between flavin-containing mono-oxygenase 3 (FMO3) genotype and trimethylaminuria phenotype in a Japanese populationBr J Clin Pharmacol775839-8512014
Miller NB,et al.Transient massive trimethylaminuria associated with food protein-induced enterocolitis syndromeJIMD Rep12011-152014
Messenger J,et al.A review of trimethylaminuria: (fish odor syndrome)J Clin Aesthet Dermatol61145-482013