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A genetic marker linked to a type of hair loss was found in most patients studied.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The patient's scalp plaques were caused by impetigo and successfully treated with antibiotics.

The girl has an inflammatory type of scarring hair loss.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

A 15-year-old boy was correctly diagnosed with a rare skin condition after initially being misdiagnosed.

Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

FFA and FAPD might be related or stages of the same disease.

Trichotillomania may have a genetic link to psychiatric disorders.

A 42-year-old woman had a scalp lesion that didn't cause hair loss and showed specific changes under a microscope.

Skin cysts might help advance stem cell treatments to repair skin.

Keratin 17 is important for hair and nail structure and affects pachyonychia congenita symptoms.

Triangular temporal alopecia can occur in adults and should be correctly identified to prevent misdiagnosis.

The man's scalp tightness after hair surgery affects his life and work, and it's unclear if it's due to the surgery or a mental health issue.

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.

Bubble hair deformity may be caused by hair shaft trauma and can improve with gentle hair care.

K15 is a reliable marker for studying stem cells in dog hair follicle tumors.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.