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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Isotretinoin reduced inflammation in tufted hair folliculitis, but hair tufting remained.

Ovarian hyperthecosis can cause polycythemia, and surgery can normalize symptoms.

Removing both ovaries can treat increased testosterone and related symptoms in postmenopausal women with ovarian hyperthecosis.

Lymphatic vessels help hair follicles regenerate by interacting with stem cells.

Topical eflornithine helps maintain hair reduction after IPL therapy in women with facial hirsutism.

Acyclovir can prevent rejection of skin grafts in herpes-related lip leucoderma.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.

Human hair follicle stem cells can help treat bone loss in osteoporosis.

RK81 can help promote hair growth.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.

A rare hair regrowth pattern can occur in some people with alopecia areata.

Iron deficiency anemia can cause hair breakage.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Surgery on a 68-year-old woman with an ovarian tumor led to reduced hirsutism and normal testosterone levels.

A hereditary condition causes hair loss and twisted hair in some family members.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Oestrogen and thyrotropin-releasing hormone affect prolactin and its receptor in human skin and hair, suggesting new treatment options for related conditions.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

Tissue-resident memory T cells can protect against infections and cancer but may also contribute to autoimmune diseases.