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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Two patients with lupus had an unusual type of hair loss not typical for the disease.

Multiple trichofolliculomas can look like multiple trichoepitheliomas on the face.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The young goat had anaplasmosis and copper deficiency.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Better diagnostic tools and treatment guidelines are needed for segmental vitiligo and related pigment issues.

A boy's scalp infection, usually found on the body, was effectively treated with antifungal cream.

The girl has a genetic hair condition causing thin hair since childhood.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

Melasma results from changes in the skin's pigment and structure, not just pigment cell growth.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Hair casts on the scalp may be a sign of ongoing pemphigus vulgaris and could suggest a need to adjust treatment.

Surgical removal of eyelid mass showed it was non-cancerous, with no recurrence after one year.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Alopecia areata can show unusual red-dotted vessels and dithranol treatment may mask typical patterns.

Using cidofovir cream for a rare skin disease can cause skin darkening.

Mice with extra sheep genes had hair that fell out and regrew in cycles.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Facial hyperpigmentation improved with oral isotretinoin and ivermectin cream after Demodex mites were identified as the cause.

Vitiligo and alopecia areata may share common causes.