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Article in Russian | MEDLINE | ID: mdl-3811724

ABSTRACT

The results of a 12 month follow-up of 3 groups of age-matched children (7 boys in each group) with an identically malignant course of Duchenne's myodystrophy determined by means of a genealogical analysis are presented. The fastest progression of the disease was observed in children receiving conventional treatment. Untreated children showed slower progression of the disease. In patients on allopurinol treatment the process was somewhat checked or there was some regression of symptomatology.


Subject(s)
Muscular Dystrophies/genetics , Allopurinol/therapeutic use , Child , Combined Modality Therapy , Follow-Up Studies , Humans , Male , Methandrostenolone/therapeutic use , Muscular Dystrophies/diagnosis , Muscular Dystrophies/therapy , Nandrolone/analogs & derivatives , Nandrolone/therapeutic use , Nandrolone Decanoate , Neostigmine/therapeutic use , Syndrome , Vitamins/therapeutic use
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