Results 11 to 20 of about 15,119 (217)

Reversible hypopigmentation with pazopanib

open access: yesIndian Journal of Medical and Paediatric Oncology, 2018
Tablet Pazopanib known to cause Hypo pigmentation and Hyperpigmentation as per various literature reports. We report here a case of reversible hypopigmentation with Pazopanib in a patient treated for spindle cell sarcoma.
B J Srinivasa   +3 more
doaj   +2 more sources

A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle [PDF]

open access: yesBMC Genetics, 2017
Background Eye pigmentation abnormalities in cattle are often related to albinism, Chediak-Higashi or Tietz like syndrome. However, mutations only affecting pigmentation of coat color and eye have also been described.
Anne K. Hollmann   +6 more
doaj   +2 more sources

Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation

open access: yesCell Reports, 2016
Reduced ocular pigmentation is common in Angelman syndrome (AS) and Prader-Willi syndrome (PWS) and is long thought to be caused by OCA2 deletion. GABRB3 is located in the 15q11-13 region flanked by UBE3A, GABRA5, GABRG3, and OCA2.
Terry Jo V. Bichell   +2 more
exaly   +3 more sources

Skin Hypopigmentation in Hematology Disorders [PDF]

open access: yesHematology Reports
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
core   +5 more sources

Correlation of Dermatology Life Quality Index and Vitiligo Extent Tensity Index: A Cross-sectional Study [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2022
Introduction: Vitiligo is a chronic depigmentary disorder having an autoimmune aetiology. Vitiligo has a severe impact on the quality of life of the individual in our country. Considering the changing socio-economic trend and the arrival of new medicines
Naveen Netaji Rao   +2 more
doaj   +1 more source

Pigmentary abnormality without significant drusen as a risk factor for late age-related macular degeneration

open access: yesScientific Reports, 2022
We investigated the incidence and risk factors of late age-related macular degeneration (AMD) in the fellow eye (FE) without significant drusen of patients with unilateral exudative macular neovascularization (MNV).
Junwon Lee   +6 more
doaj   +1 more source

Melanogenesis and Hypopigmentation

open access: yesIndian Journal of Dermatology, 2022
Melanocytes are highly specialized dendritic cells that synthesize and store melanin in subcellular organelles called melanosomes, before transfer to keratinocytes. Melanin is a complex pigment that provides colour and photoprotection to the skin, hair and eyes.
Vinardell Martínez-Hidalgo, Ma. Pilar   +2 more
openaire   +4 more sources

Perifollicular Hypopigmentation in Systemic Sclerosis: Associations with Clinical Features and Internal Organ Involvement [PDF]

open access: yes, 2022
OBJECTIVE: To determine whether perifollicular hypopigmentation in systemic sclerosis (SSc) is associated with demographics, distinct clinical features, and autoantibody profiles.
McMahan, Zsuzsanna H   +12 more
core   +1 more source

Pigmentary changes associated with endocrine and metabolic disorders

open access: yesPigment International, 2021
Pigmentary changes in skin can act as an interface to diagnose and monitor various systemic diseases. Endocrine and metabolic disorders can directly or indirectly affect melanin synthesis pathway, thus affecting melanogenesis and skin color.
Pooja Arora, Sinu Rose Mathachan
doaj   +1 more source

OCULOCEREBRAL HYPOPIGMENTATION SYNDROME (CROSS-SYNDROME)

open access: yes, 1991
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.
ÖZKAN, HASAN, KOSE, G, UNSAL, E
core   +4 more sources

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