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Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

A woman's eyelashes grew thicker and longer after taking topiramate, but returned to normal when she stopped the medication.

Minoxidil improved hair growth in a child with a rare genetic disorder.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A medicine called tofacitinib worked to treat a hair loss condition linked with a muscle and skin disease.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

Hair shaft abnormalities can help distinguish mycosis fungoides from other skin conditions.

Trichilemmal cysts may form from hair follicle outer root sheath growth.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

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

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

Tricholemmoma is linked to Cowden syndrome and can be benign or malignant.

Cystic fibrosis can cause unusual symptoms like hair color changes, which can improve with proper treatment.

Pexidartinib often causes liver issues and fatigue, especially in women.

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

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Topical rapamycin may effectively treat fibrous papules on the face.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

KFSD causes scarring hair loss and skin roughness, mainly in males.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Hypertrichosis causes excessive hair growth and needs psychological support due to its impact on self-esteem.

KLHL24-mutant stem cells help understand skin and heart disease.

A rare skin condition was identified and planned for treatment in an elderly man.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.