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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Most orthodontic patients with missing teeth also have hair disorders.

Abnormal adrenal function is not the cause of alopecia in Pomeranians; it may be due to breed-specific hormones.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Ultrasonography improves pilomatricoma diagnosis accuracy.

Ectodysplasin-A1 is crucial for developing hair, teeth, and glands.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Spiny keratoderma may be ectopic hair formation on palms and soles.

Finasteride use during early pregnancy may cause limb deformities in babies.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

The woman had a benign bone tumor removed from her leg and remained healthy with no issues 8 years later.

Twins had rare skin cysts likely due to genetics.

Identical twins both had a rare hair loss condition, suggesting it might be genetic.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

A medication called sodium valproate likely caused a girl's hair to become kinky and dry.

A 4-year-old had a rare type of hair loss that may have a good outcome.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

A 7-year-old girl had unusually long eyelashes with no known cause or related health issues.

Nevus comedonicus is a rare skin condition with grouped open pores, sometimes linked to other body issues.

A single recessive gene causes sparse hair in certain Japanese White rabbits.