Extensive Mongolian spots associated with Hunter syndrome

Author:

Sapadin Allen N.,Friedman Ilyse S.

Publisher

Elsevier BV

Subject

Dermatology

Reference19 articles.

1. A rare disease in two brothers;Hunter;Proc R Soc Med,1917

2. Incidence of Hunter’s syndrome;Young;Hum Genet,1982

3. Incidence of mucopolysaccharidoses in Israel: Is Hunter Disease a “Jewish disease”?;Schapp;Hum Genet,1980

4. Hunter disease (MPS type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl;Clarke;Am J Hum Genet,1991

5. The mucopolysaccharidoses;Whitley,1993

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1. A novel mutation in the GALC gene causes Krabbe disease accompanied with extensive Mongolian spots in a consanguineous family;Neurological Sciences;2023-03-15

2. Pigmentary disorders;Pediatric Dermatology;2022

3. Metabolic Disorders and the Skin;Harper's Textbook of Pediatric Dermatology;2019-11-20

4. The spectrum of benign dermal dendritic melanocytic proliferations;Journal of the European Academy of Dermatology and Venereology;2019-03-14

5. A comprehensive review of Mongolian spots with an update on atypical presentations;Child's Nervous System;2018-08-06

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