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Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

A 3-year-old girl has a rare condition causing sparse hair and nail issues, with minimal improvement from treatment.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

New mutations in the hairless gene may cause hair loss and affect bone development.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

HIV-positive men who have sex with men have a higher rate of anal beta-papillomavirus infections.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

Early recognition of symptoms is crucial for treating IPEX syndrome with a stem cell transplant.

Genetic testing for EGFR mutations is crucial in similar cases.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

HPV infection is linked to better survival in advanced anal cancer, higher radiation doses improve survival, especially in HPV-negative patients, and prostaglandin E₂ pretreatment can protect mouse hair follicles from radiation damage.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

Lentiviral vector effectiveness in skin is influenced by external factors, not receptor availability.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.