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Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

Neuronatin is found in specific cells within rat testis, hair follicles, tongue, and pancreas, suggesting it has various roles in tissue development and function.

Accurate diagnosis and zinc supplements can improve life quality in acrodermatitis enteropathica, even with normal zinc levels.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

A special diet can fix hair problems in argininosuccinase deficiency.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A new gene mutation linked to a skin condition was found in a Spanish family.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

Tofacitinib citrate improved nail dystrophy and pain in patients with alopecia universalis without causing side effects.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Retinoids or their analogs could treat skin pigmentation disorders like melasma and vitiligo.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

Acetylcholine receptors might be involved in the development of acne inversa and smoking could worsen the condition.

TAK-279 effectively reduces psoriasis symptoms and is safe.

Inhibiting TYK2 can restore hair growth in alopecia areata.