Results 151 to 160 of about 34,346 (291)

PR5 VALIDATION OF THE HYPERPIGMENTATION TREATMENT SATISFACTION QUESTIONNAIRE (HPTSQ)

, 2006
Sharon Colman, S. Barrows, A Nixon, M. Nixon, Ted B. Taylor, Mark J. Atkinson, Timothy A. Miller   +6 more
openalex   +1 more source

Acquired Vitamin B12 Deficiency: Cutaneous Hyperpigmentation and Hepato-Splenomegaly in Megaloblastic Anaemia / Pancytopenia Reported in a 15-Month-Old Boy

, 2020
Faten Ahmad AlKateb, Ahmed AlEidan, Layla Bidah Algahtani, Noura Muteeb AlHowiati, Aziza AlSwayyed, Abdulaziz Khaled AlAreefy, Mazen AlGhofaily   +6 more
openalex   +2 more sources

The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 407-418, February 2026.
ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, Outi Elomaa, Sirpa Kivirikko, Leila Jeskanen, Katriina Lappalainen, Nelli Sjöblom, Juha Kere, Katariina Hannula‐Jouppi, Liisa Harjama   +10 more
wiley   +1 more source

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 521-530, February 2026.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil, Allison Daley, Emily R. Sites, Shayne M. Plourde, Jesse M. Hunter, Dennis W. Bartholomew, April N. Lehman, Daniel C. Koboldt, Rolf W. Stottmann   +8 more
wiley   +1 more source

Minocycline-Induced Hyperpigmentation

Journal of Osteopathic Medicine, 2018
Leonid, Skorin, Stephanie, Norberg
openaire   +2 more sources

Familial progressive hypo- and hyperpigmentation: A variant case

, 2012
Wen‐Yuan Zhu, Ruzhi Zhang
openalex   +1 more source

Chemotherapy-Associated Supravenous Hyperpigmentation [PDF]

, 1996
E. Baselga, Beth A. Drolet, James T. Casper, Nancy B. Esterly   +3 more
openalex   +1 more source

Asymmetric Lip Hyperpigmentation in a Transplant Patient. [PDF]

Dermatopathology (Basel)
Kimpe V, Alvarez Martinez D, Menzinger S, Kaya G.   +3 more
europepmc   +1 more source

Hyperpigmentation in palms associated with lung adenocarcinoma resolving after chemotherapy [PDF]

, 2014
Fengying Wu, Chunxia Su, Li Liu, Jianfang Xu   +3 more
openalex   +1 more source

Bilateral Idiopathic Pyoderma Gangrenosum: A Case Report of an Atypical Presentation

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Pyoderma gangrenosum (PG) is a rare non‐infectious neutrophilic dermatosis which is characterized by a rapidly progressive, painful ulcer. Bilateral manifestation of PG is exceptionally rare and can easily be misdiagnosed as infection or vascular ulceration, delaying proper treatment.
Sanjog Thapa Magar, Deekshanta Sitaula, Subi Rijal, Vikash Paudel, Bhaskar M. M. Kayastha   +4 more
wiley   +1 more source