Acanthosis nigricans: pointer of endocrine entities

AM Radu, M Carsote, MC Dumitrascu, F Sandru - Diagnostics, 2022 - mdpi.com
Acanthosis nigricans (AN) has been reported in relation to insulin resistance (IR). We aim to
review AN through an endocrine and metabolic perspective focusing on IR in association …

[HTML][HTML] H syndrome: A histiocytosis-lymphadenopathy plus syndrome. A comprehensive review of the literature

A Hamad, H Elwaheidi, F Salameh… - … /Oncology and Stem …, 2024 - journals.lww.com
H syndrome is a rare autosomal recessive genodermatosis that falls under the histiocytosis-
lymphadenopathy plus syndrome. The term “H syndrome” includes manifestations such as …

[HTML][HTML] Rheumatological manifestations of H syndrome

R Honsali, L Tahiri, S Cherkaoui-Dekkaki… - …, 2024 - pmc.ncbi.nlm.nih.gov
H syndrome (HS) is a rare autosomal recessive genodermatosis characterised by cutaneous
hyperpigmentation, hypertrichosis, sclerodermatous thickening, and multisystemic …

[HTML][HTML] H syndrome: report of the first case in African ethnicity

OKA Elmansour, AOA Babikir - Cureus, 2022 - ncbi.nlm.nih.gov
H syndrome is an autosomal recessive multisystemic disease with a very low prevalence
rate, characterized by indurated cutaneous hyperpigmentation, hypertrichosis, and various …

Syndromes with Hypomelanosis

C Tan, WY Zhu - Atlas of Pigmentary Skin Disorders, 2023 - Springer
Syndromes with hypomelanosis are introduced: Alezzandrini syndrome, Chediak–Higashi
syndrome, Griscelli syndrome, Hermansky–Pudlak syndrome, Menkes kinky hair syndrome …