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Chediak-Higashi syndrome.
Indian J Pediatr ; 2000 Aug; 67(8): 595-7
Article in English | IMSEAR | ID: sea-80153
ABSTRACT
A case of Chediak-Higashi syndrome is reported in a four-year-old boy who presented with recurrent chest infection, partial albinism, hyperpigmentation of the extremities and presence of giant granules in leucocytes and melanocytes in the skin. Parental consanguinity was present. Though uncommon, hyperpigmentation of sun exposed areas may be the initial symptom in Chediak-Higashi syndrome.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Arm / Ascorbic Acid / Blood Transfusion / Humans / Male / Chediak-Higashi Syndrome / Child, Preschool / Hyperpigmentation / Fatal Outcome / Combined Modality Therapy Language: English Journal: Indian J Pediatr Year: 2000 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Arm / Ascorbic Acid / Blood Transfusion / Humans / Male / Chediak-Higashi Syndrome / Child, Preschool / Hyperpigmentation / Fatal Outcome / Combined Modality Therapy Language: English Journal: Indian J Pediatr Year: 2000 Type: Article