Lowe syndrome: report of a case and brief literature review
Iranian Journal of Pediatrics. 2009; 19 (4): 417-420
em Inglês
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| ID: emr-99992
ABSTRACT
The oculocerebrorenal syndrome of Lowe [OCRL] is a rare x-linked recessive disorder first described in 1952. This syndrome is characterized by ocular involvement, mental retardation and kidney disease. The causative gene is OCRL1. Survival rarely exceeds 40 years. A 13-year-old boy was referred because of short stature. In physical examination his height was 108.2 cm. He had poor growth, psychomotor retardation, severe hypotonia, congenital cataract which was operated on earlier in life, searching nystagmus, anti social behavior and used foul language. He had been on treatment for renal tubular acidosis [Fanconi syndrome] since 8 month of age. The possibility of OCRL should be considered in boys with cataracts and glumerolar disease. As the condition can be diagnosed in first months of life, early treatment can prevent patients from various complications
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Acidose Tubular Renal
/
Catarata
/
Nistagmo Congênito
/
Deficiência Intelectual Ligada ao Cromossomo X
/
Genes Ligados ao Cromossomo X
/
Hipotonia Muscular
/
Transtorno da Personalidade Antissocial
Tipo de estudo:
Relato de Casos
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Iran. J. Pediatr.
Ano de publicação:
2009
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