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Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

The rash resolved after stopping ponatinib.

Obesity increases the risk of polycystic ovary syndrome and anemia in women who can have children.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

A 16-year-old girl with autoimmune hemolytic anemia and deep vein thrombosis improved with treatment, possibly indicating systemic lupus erythematosus.

Enhanced stem cells can reduce fat buildup in eye tissue for Graves' disease.

Excess maternal androgens can cause heart problems in offspring.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Ruxolitinib can cause a delayed skin reaction on the nose.

A 73-year-old woman's unusual hair loss and growth led to the discovery of a rare condition causing too much testosterone, which improved after her ovaries were removed.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Epithelial grafting can effectively repigment white hair in vitiligo patients.

Most women with hirsutism in the UAE have polycystic ovary syndrome (PCOS).

Unani medicine may help treat a rare, hard-to-treat hair loss pattern in children.

A dark-haired Chinese girl had hair that looked banded under certain light but was normal under a microscope.

Two sisters with rickets and hair loss had a genetic issue with vitamin D processing, and only improved when given phosphorus supplements.

The skin lesion was diagnosed as a matrical cyst with unusual features.

Hirsutism in young girls can have causes other than PCOS, so diagnoses should be reassessed if treatments don't work.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.