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Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups.
Moser, A B; Rasmussen, M; Naidu, S; Watkins, P A; McGuinness, M; Hajra, A K; Chen, G; Raymond, G; Liu, A; Gordon, D.
Afiliação
  • Moser AB; Kennedy Krieger Institute, Baltimore, MD 21205, USA.
J Pediatr ; 127(1): 13-22, 1995 Jul.
Article em En | MEDLINE | ID: mdl-7541833
OBJECTIVE: To use the technique of complementation analysis to help define genotype and classify patients with clinical manifestations consistent with those of the disorders of peroxisome assembly, namely the Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and rhizomelic chondrodysplasia punctata (RCDP). STUDY DESIGN: Clinical findings, peroxisomal function, and complementation groups were examined in 173 patients with the clinical manifestations of these disorders. RESULTS: In 37 patients (21%), peroxisome assembly was intact and isolated deficiencies of one of five peroxisomal enzymes involved in the beta-oxidation of fatty acids or plasmalogen biosynthesis were demonstrated. Ten complementation groups were identified among 93 patients (54%) with impaired peroxisome assembly and one of three phenotypes (ZS, NALD, or IRD) without correlation between complementation group and phenotype. Forty-three patients (25%) had impaired peroxisome assembly associated with the RCDP phenotype and belonged to a single complementation group. Of the 173 patients, 10 had unusually mild clinical manifestations, including survival to the fifth decade or deficits limited to congenital cataracts. CONCLUSIONS: At least 16 complementation groups, and hence genotypes, are associated with clinical manifestations of disorders of peroxisome assembly. The range of phenotype is wide, and some patients have mild involvement.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndrome de Zellweger / Doença de Refsum / Adrenoleucodistrofia / Microcorpos Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Pediatr Ano de publicação: 1995 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndrome de Zellweger / Doença de Refsum / Adrenoleucodistrofia / Microcorpos Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Pediatr Ano de publicação: 1995 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos