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Some overweight or obese men with long-term frontal fibrosing alopecia may have abnormal sex hormone levels.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Various potential triggers may be causing the rise in frontal fibrosing alopecia, and avoiding these could help stop the disease's increase.

A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

Acitretin effectively improved the woman's skin condition.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

Neutered ferrets often develop hyperadrenocorticism, with symptoms like hair loss and lethargy, and androstenedione is a key indicator for diagnosis.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

A 16-year-old boy with Castleman's disease and lupus was successfully treated and showed no recurrence.

Ichthyoses are genetic skin disorders that affect the skin's barrier function.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

A woman with lupus developed rare skin growths that went away on their own.

Accurate diagnosis of pseudolymphomatous folliculitis is crucial to avoid mistaking it for more serious conditions.

Adrenal gland disease is common in ferrets and causes hair loss and other symptoms.

Early diagnosis and treatment of frontal fibrosing alopecia are crucial to prevent permanent hair loss.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The document suggests more research is needed to understand skin conditions related to toothpaste and other treatments.

FGF5 gene mutations cause long hair in domestic cats.

Early diagnosis and treatment are crucial for managing Folliculotropic Mycosis Fungoides on the scalp.

A young man had a rare skin condition causing hair loss and forehead lesions.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Goats may need lifelong zinc supplements due to hereditary zinc absorption issues.