Familial Richner‐Hanhart syndrome: Report of a sibling with incomplete presentation
Author:
Affiliation:
1. Skin Research Center Shohada‐e Tajrish Hospital, Shahid Beheshti University of Medical Sciences Tehran Iran
2. Department of Pathology Hamedan University of Medical Sciences, Besat Hospital Hamedan Iran
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/dth.14072
Reference9 articles.
1. The hereditary palmoplantar keratoses: an updated review and classification
2. Richner-Hanhart syndrome (Tyrosinemia Type II) Case report and literature review
3. Richner‐Hanhart syndrome (tyrosinemia type II): a case report of delayed diagnosis with pseudodendritic corneal lesion;Iskeleli G;Turk J Pediatr,2011
4. Plantar keratoderma: a manifestation of tyrosinemia type II (Richner-Hanhart Syndrome)
5. Richner-Hanhart Syndrome (Tyrosinemia II): Early Diagnosis of an Incomplete Presentation with Unusual Findings
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