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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Combining PRP injections with minoxidil 2% effectively promotes hair growth in hereditary hair loss.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Minoxidil helps 32% of patients with hereditary baldness regrow hair.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Using minoxidil on the scalp can help grow hair for people with hereditary baldness.

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

Researchers found a gene mutation responsible for a rare hair loss condition.

A new mutation in the HR gene causes hair loss in a specific family.

Monilethrix is a rare genetic hair disorder that's hard to treat.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Some treatments like minoxidil, finasteride, and surgery can help with hereditary hair loss.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.