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A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Amelanotic melanocytes from hair follicles are immature and likely don't transfer melanosomes to keratinocytes.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Researchers found three patterns of Frontal fibrosing alopecia, with Pattern III having the best prognosis after treatment.

The condition is likely inherited in an autosomal-dominant pattern.

AP-1 controls tumor cell type by affecting key signaling pathways.

Scientists made stem cells that can grow hair by adding three specific factors to them.

Recognizing unusual patterns of hair loss helps dermatologists diagnose and manage Alopecia Areata better.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

Congenital atrichia with papular lesions causes permanent hair loss in children.

HAP stem cells can repair nerves and spinal cords by becoming Schwann cells.

Treatment improved scalp conditions and hair loss with no recurrence after 1 year.

CD3+ T-cell presence is a reliable marker to tell apart alopecia areata from pattern hair loss.

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

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Some families have a genetic condition where they are born with irregular scalp defects.

Hair density and thickness decrease in all scalp areas for East Asians with AGA.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

The girl's thin hair was due to loose anagen syndrome, not other hair loss types.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

Type IV collagen chains vary in different parts of human skin, with specific patterns linked to melanocytes.

Sudden, unusual hair loss may indicate serious underlying health issues.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.