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A rare ovarian tumor caused a postmenopausal woman to develop male-like features, which improved after surgery.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

Tofacitinib may be an effective and safe treatment for hair loss in teenagers with alopecia areata.

Trichoscopy is crucial for diagnosing and assessing alopecia areata in children.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Topical minoxidil and tretinoin improved hair growth in a girl with EDSS1 over two years.

Hair transplantation effectively treated a bald patch in an 18-year-old woman with Temporal Triangular Alopecia.

Excessive eyelash growth from erlotinib may indicate positive tumor response and help treat madarosis.

A rare ovarian tumor caused early puberty signs in a 1-year-old girl, but surgery reduced hormone levels.

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

A 17-year-old girl was diagnosed with a rare ovarian tumor, emphasizing the need for fertility preservation and psychosocial care.

An 8-year-old with severe hair loss regrew all hair after six months of tofacitinib treatment.

The boy's symptoms suggest a possible new medical condition.

Treating both bipolar disorder and hair-related BDD with psychiatric medications improved the patient's symptoms.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.

A 17-year-old boy with Temporal Triangular Alopecia successfully grew new hair after a hair restoration surgery using follicular unit transplantation.

Tofacitinib helped psoriasis but not alopecia universalis, needing more research.

Surgery removed ovarian tumors, normalizing testosterone and improving symptoms.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

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

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Pertussis toxin may contribute to hair loss in alopecia areata.

A runner developed tangled armpit hairs from shirt friction, preventable by shaving or wearing smooth shirts.

Emotional stress can trigger intermittent hair loss in chronic telogen effluvium, which may not improve with treatment if stress continues.

Trichofolliculoma was found in a person with amniotic band syndrome for the first time.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.