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Researchers created early-stage hair-like structures from skin cells, showing how these cells can self-organize, but more is needed for complete hair growth.

Keloids can form at the site of a healed herpes zoster infection, but the reason is unclear.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

A postmenopausal woman's hirsutism and high testosterone levels improved after surgery for an ovarian tumor not seen on ultrasound.

Mesothelioma of the tunica vaginalis testis is rare, often high-grade, and has a median survival of about 24 months.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Alopecia can be caused by multicentric reticulohistiocytosis.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Exosomes from fat-derived stem cells help repair large bone defects by attracting and enhancing bone marrow stem cells.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

The procedure effectively removes forehead osteomas with minimal scarring and no complications.

A rare calcium deposit condition was found on a man's scalp.

Targeting adipocyte-to-mesenchymal transition could help treat fibrosis.

Hirsutism in young girls can have various causes beyond PCOS, so diagnoses should be reconsidered if treatments don't work.

Custom-designed implants effectively repaired skull damage in most soldiers injured in combat.

A specific gene mutation causes a severe skin disorder in a family.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

A woman's masculine symptoms were caused by a rare tumor in her left ovary, which was found using a special blood test.

Increased ODC activity leads to skin tumors by recruiting stem cells, not by toxic byproducts.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

A mutation in the KRTHB5 gene causes hair and nail issues.

Thyroid hormone therapy effectively treated the man's rare muscle and heart issues.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.