Soelatin Winarno
Department of Child Health, Universitas Diponegoro Medical School/Dr. Kariadi Hospital, Semarang, Central Java

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Cerebral Palsy in Y .P .A. C. (Institution for Crippled Children) Semarang Soelatin Winarno; Oemar Wirjohatmodjo; Harijono Harijono; Siti Alfinah; Wirawan Wirawan
Paediatrica Indonesiana Vol 16 No 9-10 (1976): September - October 1976
Publisher : Indonesian Pediatric Society

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (487.998 KB) | DOI: 10.14238/pi16.9-10.1976.330-6

Abstract

Thirty-five cases of cerebral palsy patients admitted to the Institution for Crippled Children, Semarang, have been discussed. Diagnosis was made by a team comprising an orthopedic surgeon, a neurologist, a paediatrician, and a psychologist. Treatment performed consisted of muscle relaxant, physiotherapy, and also surgery. Introduction, material arid method of observation, treatment, sex distribution; classification, speech disturbance, mental status, results of treatment, and comparison with the cases in Bombay, form the sequence of this report.
Progressive Muscular Dystrophy (Duchenne Type) (Case Report) Soelatin Winarno; Indrawarman Indrawarman; Sabdo Waloejo; Lydia Kristianti
Paediatrica Indonesiana Vol 16 No 9-10 (1976): September - October 1976
Publisher : Indonesian Pediatric Society

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (493.556 KB) | DOI: 10.14238/pi16.9-10.1976.361-4

Abstract

Clinical findings of two brothers suffering from progressive muscular dystrophy pseudohypertrophic type according to Duchenne are reported. Literatures dealing with its clinical classification, biochemical disturbances, hypotheses of the pathogenesis, management of treatment, mode of action of A.T.P. and the pedigree have been briefly reported. Progressive Muscular Dystrophy is a progressive disease affecting voluntary muscles; It is characterized by a decreased strength in the affected muscles with rapid or slow gradual progression. About 45% of the patients gave a history that at least another member of the family is affected by the disease. Pseudohypertrophic form (Duchenne type) is usually inherited as a recessive factor, often sexlinked.