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Iron supplements may reverse premature graying in iron-deficient individuals; ingrown nails are common in diabetics with certain risk factors; topical finasteride may reduce scalp DHT as effectively as oral finasteride; monilethrix treatment is challenging but some medications can help.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Eyebrow mesotherapy improves eyebrow appearance and boosts confidence and mood.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

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

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Zinc supplements and weaning cured a breast-fed baby's zinc deficiency caused by a gene mutation.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Almost all patients with chronic kidney disease not yet on dialysis have at least one skin problem.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

Poor nutrition in young children causes skin and hair issues, highlighting the need for better nutrition education.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

The procedure is effective for reducing the forehead despite potential for visible scars.

Restoring phenylalanine levels improved skin and hair symptoms in a PKU infant.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Hair examination helps diagnose rare neurological diseases in children.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.