Literature DB >> 15283796

Elejalde syndrome: report of a case and review of the literature.

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.

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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


  3 in total

Review 1.  Disorders of lysosome-related organelle biogenesis: clinical and molecular genetics.

Authors:  Marjan Huizing; Amanda Helip-Wooley; Wendy Westbroek; Meral Gunay-Aygun; William A Gahl
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

2.  [Hereditary pigmentary disorders].

Authors:  K Giehl; M Braun-Falco
Journal:  Hautarzt       Date:  2010-07       Impact factor: 0.751

3.  Silvery hair syndrome in two cousins: Chediak-Higashi syndrome vs Griscelli syndrome, with rare associations.

Authors:  R Raghunatha Reddy; Balaji M Babu; B Venkateshwaramma; Ch Hymavathi
Journal:  Int J Trichology       Date:  2011-07
  3 in total

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