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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

Anorexia nervosa may cause a hair defect called pili torti due to malnutrition and high vitamin A levels.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Obstructive sleep apnea can be hereditary and linked to a genetic mutation in the COL1A2 gene.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

The document concludes that understanding the evolution of the human face helps cosmetic surgeons meet aesthetic desires.

Mesenchymal MEIS2 is essential for whisker development without needing sensory nerves.

A chubby child can still be malnourished.

New mutations in the hairless gene may cause hair loss and affect bone development.

Dental erosion is common in adolescents and is linked to diet and higher socioeconomic status.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

JAK inhibitors help hair regrowth but not fully effective for androgenetic alopecia.

A 12-year-old boy has a rare, harmless hair loss on his chin with no need for treatment.

Pax9 is crucial for proper tongue surface development and preventing skin-like changes.

The big-clawed shrew's sinus hair follicles are highly specialized for sensing vibrations.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Accurate diagnosis and management of rare genian fistulas require combined clinical, radiologic, and histopathologic evaluations.

Different fish use the same genes to regrow teeth.

Janus kinase inhibitors can help children with alopecia areata regrow hair but may have some risks.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.