Literature DB >> 26337734

Griscelli Syndrome Type 3: Two New Cases and Review of the Literature.

Ariella Nouriel1, Jonah Zisquit1, Alexander M Helfand1, Yair Anikster2, Shoshana Greenberger1.   

Abstract

A 3-year-old Arab boy with a history of hypoplastic left heart syndrome was referred to the pediatric dermatology clinic at Sheba Medical Center for evaluation of hypomelanosis, manifested by fair skin pigmentation and silvery-grey hair, eyebrows, and eyelashes. The child had one older brother with similar hypopigmentation and another older brother who had died of congenital heart disease. The child had no history of neurologic deficits or immunodeficiency and no additional findings on clinical evaluation.
© 2015 Wiley Periodicals, Inc.

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Year:  2015        PMID: 26337734     DOI: 10.1111/pde.12663

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  2 in total

1.  [Differential diagnostics of hypomelanoses].

Authors:  M Böhm
Journal:  Hautarzt       Date:  2015-12       Impact factor: 0.751

Review 2.  [Oculocutaneous and ocular albinism].

Authors:  A S Kubasch; M Meurer
Journal:  Hautarzt       Date:  2017-11       Impact factor: 0.751

  2 in total

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