Results 131 to 140 of about 19,181 (266)
Oculocerebral hypopigmentation syndrome (Cross syndrome).
A typical case of Cross syndrome with hypopigmentation, mental and psychomotor retardation, spasticity, bilateral optic atrophy and dental defects in a three-year-old boy is presented. The clinical features of this rare syndrome are discussed.
ÖZKAN, HASAN, UNSAL, E, KOSE, G
openaire +3 more sources
Skin Hypopigmentation in Hematology Disorders
Hypopigmentation disorders pose significant diagnostic challenges in dermatology, sometimes reflecting underlying hematological conditions. This review explores the clinical presentations related to hypopigmentation in hematological disorders, focusing on vitiligo, morphea, and syndromic albinism. Vitiligo, an autoimmune disorder targeting melanocytes,
Roberto Mazzetto +4 more
openaire +3 more sources
Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
Folliculotropic mycosis fungoides (FMF) is a rare subtype of MF, characterized by prominent folliculotropism in histopathology. Clinically, FMF exhibits polymorphic presentations, mainly including follicular papules, plaques, alopecia, and other nonspecific lesions, with a predilection for the head and neck region, leading to frequent misdiagnosis ...
Xingyu Li, Jie Liu, Nicola Pimpinelli
wiley +1 more source
Possible role of psoralen-induced phototoxicity in the development of vitiligo
Genevieve Patrick, BS +4 more
doaj +1 more source
Key Clinical Message Tetraploid–diploid mosaicism in humans is exceedingly rare. We present an 11‐year‐old boy with tetraploid–diploid mosaicism and coexistent hair hypopigmentation with skin hypo‐ and hyperpigmentation.
John Paul Schacht +3 more
doaj +1 more source
Oculocerebral Hypopigmentation Syndrome Maps to Chromosome 3q27.1q29 [PDF]
Elyes Chabchoub +5 more
openalex +1 more source
Hypopigmentation-punctate palmoplantar keratoderma syndrome [PDF]
INSERM
openalex +1 more source
Défaut d’exocytose des granules lytiques : Plusieurs causes, un même effet [PDF]
Une réponse immune exagérée, incontrôlée et le plus souvent fatale, connue sous le nom de syndrome hémophagocytaire (SH), est associée à un défaut de la fonction cytotoxique des lymphocytes T et natural killer (NK).
de Saint Basile, Geneviève +4 more
core
Frontiers in Pigment Cell and Melanoma Research
We identify emerging frontiers in clinical and basic research of melanocyte biology and its associated biomedical disciplines. We describe challenges and opportunities in clinical and basic research of normal and diseased melanocytes that impact current ...
Birlea, Stanca +26 more
core +1 more source

