Bilateral harlequin syndrome, unilateral Horner syndrome, and Riga‐Fede disease as presenting features of hereditary sensory and autonomic neuropathy type IV-Reference-Cited by-同舟云学术

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Bilateral harlequin syndrome, unilateral Horner syndrome, and Riga‐Fede disease as presenting features of hereditary sensory and autonomic neuropathy type IV

Published:2020-09-28 Issue:1 Volume:38 Page:213-216
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Alobaida Saud¹²^ORCID,Lam Joseph M.¹³^ORCID

Affiliation:

1. Department of Dermatology and Skin Sciences University of British Columbia Vancouver BC Canada

2. Department of Dermatology King Faisal Specialist Hospital & Research Centre Riyadh Saudi Arabia

3. Department of Pediatrics and Department of Dermatology and Skin Sciences University of British Columbia Vancouver BC Canada

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14385

Reference18 articles.

1. Recent advances in hereditary sensory and autonomic neuropathies

2. Disease mechanisms in hereditary sensory and autonomic neuropathies

3. Phenotypes and Genotypes in Five Children with Congenital Insensitivity to Pain with Anhidrosis

4. An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis;Bonkowsky JL;Pediatrics,2003

5. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation

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