ArticleMedicina (Kaunas, Lithuania)2019
Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes.
Article in Medicina (Kaunas, Lithuania), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Gray Hair: From Preventive to Treatment.Clinical, cosmetic and investigational dermatology · 2025Review
- Griscelli syndrome: a diagnostic challenge of a rare disease: a case report.Annals of medicine and surgery (2012) · 2024Article
- Silver hair in a neonate: a tale of 2 fatal cases.Oxford medical case reports · 2024Article
- cDNA sequencing increases the molecular diagnostic yield in Chediak-Higashi syndrome.Frontiers in genetics · 2023Article
- Candidate pigmentation genes related to feather color variation in an indigenous chicken breed revealed by whole genome data.Frontiers in genetics · 2022Article
- Hair Shaft Examination: A Practical Tool to Diagnose Griscelli Syndrome.Dermatopathology (Basel, Switzerland) · 2021Article
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Authors and funding
11 authors.
Funding
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Abstract
The term congenital hypopigmentary disorders refers to a wide group of heterogeneous hereditary diseases, clinically characterized by inborn pigmentary defects of the iris, hair, and/or skin. They include Gray Hair Syndromes (GHSs), a rare group of autosomal recessive genodermatosis hallmarked by inborn silvery gray hair. GHSs encompass Griscelli, Chediak⁻Higashi, Elejalde, and Cross syndromes, which are all characterized by a broad spectrum of severe multisystem disorders, including neurological, ocular, skeletal, and immune system impairment. In this manuscript, we describe in detail the clinical, trichoscopic, and genetic features of a rare case of Griscelli syndrome; moreover, we provide an overview of all the GHSs known to date. Our report highlights how an accurate clinical examination with noninvasive methods, like trichoscopy, may play a crucial rule in diagnosis of rare and potentially lethal genetic syndromes such as Griscelli syndrome, in which timely diagnosis and therapy may modify the clinical course, quality of life, and likelihood of survival.
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