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Indian Pediatr ; 2004 Sep; 41(9): 944-7
Article in English | IMSEAR | ID: sea-13863

ABSTRACT

An infant with partial albinism was suspected to have Chediak-Higashi syndrome because two of his elder siblings had albinism and died in childhood following accelerated phase. Detailed investigations of blood, hair and skin of the proband revealed that he had Griscelli syndrome.


Subject(s)
Chediak-Higashi Syndrome/diagnosis , Codon, Nonsense , Diagnosis, Differential , Humans , Immunologic Deficiency Syndromes/genetics , Infant, Newborn , Male , Melanocytes/pathology , Piebaldism/genetics , Prognosis , rab GTP-Binding Proteins/genetics
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