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A 2-year-old boy with hypoactivity of neonatal onset and profound developmental delay

✍ Scribed by Masashi Mizuguchi; Masayuki Itoh; Hiroshi Ozawa; Yukihiko Morikawa


Book ID
108957923
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
276 KB
Volume
27
Category
Article
ISSN
0919-6544

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We report a 2-year-old boy with Duchenne muscular dystrophy (DMD), glycerol kinase deficiency (GK) and adrenal hypoplasia congenita (AHC). At three weeks of age, the patient was hospitalized for the first time with symptoms of hypotone dehydration because of AHC. At present, he shows severe muscular