| Literature DB >> 15283796 |
Juliana Burihan Cahali1, Solange Assuncion Villagra Fernandez, Zilda Najjar Prado Oliveira, Maria Cecília da Mata Rivitti Machado, Neusa Sakai Valente, Mírian Nacagami Sotto.
Abstract
Elejalde syndrome is a rare autosomal recessive condition, with only 10 reported cases through 2001. It is characterized by silvery hair, pigment abnormalities, and profound central nervous system dysfunction. The differential diagnosis includes Griscelli and Chediak-Higashi syndromes, which present with silvery hair, pigment abnormalities, central nervous system alterations, and severe immunologic dysfunction. We report a 6-year-old girl with Elejalde syndrome and review Elejalde, Griscelli, and Chediak-Higashi syndromes.Entities:
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Year: 2004 PMID: 15283796 DOI: 10.1111/j.0736-8046.2004.21414.x
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588