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Geriatric Julia Creek dunnarts often suffer from reproductive and skin diseases, impacting conservation efforts.

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The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

UVB radiation changes the levels of certain microRNAs in skin cells, which may affect cell survival and hair growth.

DVI provides detailed 3D imaging of hair and shows how various products protect and enhance hair.

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The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

Keratin 19 may help diagnose and treat certain types of permanent hair loss.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Ultrasonic microneedles improve hair regrowth treatment effectiveness without side effects.

A medicine called tofacitinib worked to treat a hair loss condition linked with a muscle and skin disease.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

Specific gene variants affect wool traits in Chinese Tan sheep.

Manfred Lucas, MD, lived from 1938 to 1997.

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

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A new gene, JMJD1C, may affect testosterone levels in men.

Bim and Puma proteins are found in developing mouse hair follicles and are involved in more than just cell death.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

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Follicular dystrophy in immunocompromised patients may be linked to medication or viral factors and can improve with treatment changes.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

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