- Case Report
- A Case of Werdnig-Hoffmann Disease.
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C H Koo, G J Lee, H G Jung, U J Jung, B Huh, M H Huh
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Clin Exp Pediatr. 1987;30(10):1170-1175. Published online October 31, 1987
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A case of Werdnig-Hoffmann disease (Kugelberg-Welander type), rare neuromuscular disease in
childhood, was presented in a 11 years old Korean boy.
The patient was well until 3yrs of age, when he was found to have muscle weakness of both upper
and lower extremity. At the time of admission he showed emaciated, and flaccid apperance with
tongue fasciculation.
Diagnosis was established by clinical teature, eletromyography, and... |
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- A Case of Congenital Hypoplastic Anemia.
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D S Moon, D K Na, J D Jo, I S Jun, M H Huh
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Clin Exp Pediatr. 1983;26(5):499-503. Published online May 31, 1983
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The Authors report A Case of Congenital Hypoplastic Anemia with congenital megacoloit
in a about one month old male infant who was admitted because of abdominal distension,
failure of passing meconium for 96 hours and pale anemic face. This syndrome was diagnosed
by clinical and laboratory findings: normochromic anemia, reticulocytopenia, developing early
infant, bone marrow with normal cellularity and deficiency of red cell precursor.
A... |
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