Albinism Latest Advances

A participatory systematic review on human rights and the birth of a child with albinism in sub-Saharan Africa.

Journal: Women's health (London, England)

Published: December 11, 2025

Analysis of multi-trait evolution across independently evolved cavefish populations reveals shared and independent evolution of suites of cave-associated traits.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Ampyrone (4-Aminoantipyrine) is a Direct Agonist of Human Tyrosinase and Potential Therapeutic for Oculocutaneous Albinism and Disorders of Hypopigmentation.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

A novel homozygous HPS4 mutation in Hermansky-Pudlak syndrome: case report and literature review.

Journal: Therapeutic advances in respiratory disease

Published: November 24, 2025

Climate Change and Dermatologic Diseases in the Global South: A Rising Challenge.

Journal: Dermatologic clinics

Published: November 09, 2025

Female Carrier of Ocular Albinism Linked to Gpr143 Gene.

Journal: Journal of vitreoretinal diseases

Published: November 03, 2025

Hermansky-Pudlak Syndrome.

Journal: Clinics in chest medicine

Published: October 19, 2025

Alterations of Photoreceptor Synaptic Ribbons in the Retina of a Human Patient With Oculocutaneous Albinism Type 1 (OCA1).

Journal: Investigative ophthalmology & visual science

Published: October 08, 2025

Topical Treatments for Rare Genetic Dermatological Diseases: A Narrative Review.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: October 02, 2025

TYROSINASE-Deficient Human Retinal Pigment Epithelium Exhibits Melanosome Maturation Defects.

Journal: Investigative ophthalmology & visual science

Published: October 01, 2025

Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations.

Journal: The Journal of dermatology

Published: September 29, 2025

Spontaneous mutant in threespine stickleback connects endosome trafficking disorders and inflammatory bowel diseases via changes in the gut microbiome.

Journal: bioRxiv : the preprint server for biology

Published: September 26, 2025

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A participatory systematic review on human rights and the birth of a child with albinism in sub-Saharan Africa.

A participatory systematic review on human rights and the birth of a child with albinism in sub-Saharan Africa.

Analysis of multi-trait evolution across independently evolved cavefish populations reveals shared and independent evolution of suites of cave-associated traits.

Analysis of multi-trait evolution across independently evolved cavefish populations reveals shared and independent evolution of suites of cave-associated traits.

Ampyrone (4-Aminoantipyrine) is a Direct Agonist of Human Tyrosinase and Potential Therapeutic for Oculocutaneous Albinism and Disorders of Hypopigmentation.

Ampyrone (4-Aminoantipyrine) is a Direct Agonist of Human Tyrosinase and Potential Therapeutic for Oculocutaneous Albinism and Disorders of Hypopigmentation.

A novel homozygous HPS4 mutation in Hermansky-Pudlak syndrome: case report and literature review.

A novel homozygous HPS4 mutation in Hermansky-Pudlak syndrome: case report and literature review.

Climate Change and Dermatologic Diseases in the Global South: A Rising Challenge.

Climate Change and Dermatologic Diseases in the Global South: A Rising Challenge.

Female Carrier of Ocular Albinism Linked to Gpr143 Gene.

Female Carrier of Ocular Albinism Linked to Gpr143 Gene.

Hermansky-Pudlak Syndrome.

Hermansky-Pudlak Syndrome.

Alterations of Photoreceptor Synaptic Ribbons in the Retina of a Human Patient With Oculocutaneous Albinism Type 1 (OCA1).

Alterations of Photoreceptor Synaptic Ribbons in the Retina of a Human Patient With Oculocutaneous Albinism Type 1 (OCA1).

Topical Treatments for Rare Genetic Dermatological Diseases: A Narrative Review.

Topical Treatments for Rare Genetic Dermatological Diseases: A Narrative Review.

TYROSINASE-Deficient Human Retinal Pigment Epithelium Exhibits Melanosome Maturation Defects.

TYROSINASE-Deficient Human Retinal Pigment Epithelium Exhibits Melanosome Maturation Defects.

Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations.

Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations.

Spontaneous mutant in threespine stickleback connects endosome trafficking disorders and inflammatory bowel diseases via changes in the gut microbiome.

Spontaneous mutant in threespine stickleback connects endosome trafficking disorders and inflammatory bowel diseases via changes in the gut microbiome.