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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Socket preservation helps maintain bone for future dental implants after tooth extraction.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

The first pediatric case of naevus trichilemmocysticus was documented.

Leukemia can sometimes appear as unusual skin issues in children.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A 15-year-old boy's skin and hair condition worsened due to improper treatment, leading to severe health issues.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

High levels of cortisol in hair are linked to a greater risk of brain aneurysm rupture.

A rare skin tumor with bone formation was successfully removed without recurrence.

Isotretinoin can cause rare scalp cysts and hair loss, treatable with medication.

Two siblings have a rare hair condition caused by a new genetic variant.

Forehead reduction and orbital contouring are important for satisfactory facial feminization in transgender females, with high satisfaction and low long-term problems.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

A rare scalp condition caused scarring hair loss in a woman, improved slightly with treatment.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

Dissecting Cellulitis of the Scalp is more common in young men and often associated with head and neck acne.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

Premature hair graying in the face may be influenced by genetics and environment.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

A toddler with a rare adrenal gland tumor causing male-like physical changes was successfully treated with surgery.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

The 6-year-old Somalian girl fully recovered from her symptoms after successful surgery and treatment.