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  • Title: [Wiskott-Aldrich syndrome: Case report].
    Author: Pacheco-Rosas D, Pomerantz A, Blachman-Braun R.
    Journal: Arch Argent Pediatr; 2015 Jun; 113(3):e137-9. PubMed ID: 25996331.
    Abstract:
    The Wiskott-Aldrich syndrome is a rare X-linked recessive immunodeficiency, with an estimated incidence of 3.5 to 5.2 cases per million males. It is characterized by immunodeficiency, microthrombocytopenia and eczema. We present a 5-year-old Hispanic male, with a medical history of numerous infectious diseases, compromised health, chronic malnutrition, language delay and failure to thrive. An infrequent mutation in the Wiskott-Aldrich syndrome gene was found.
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