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A Persian cat had a rare skin condition that didn't improve with treatment.

PEA reduces pain by increasing neurosteroid synthesis in the spinal cord.

Chinese patients with primary cicatricial alopecia often have folliculitis decalvans, benefit from treatment, but may experience relapse, with dermoscopy being a useful diagnostic tool.

Pica disorder in central Iraq is mainly found in females and is linked to low iron levels; treatment with iron improves most patients.

A patient with PPP had rare skin reactions to adalimumab, which improved after stopping smoking and continuing acitretin.

Severe CCCA may be biologically and clinically different from milder forms.

An antibiotic called co-trimoxazole can effectively treat autoimmune diseases.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Long COVID can cause lasting health issues like fatigue and brain fog, especially in those with severe initial infections or no vaccination.

Trichodynia is a painful scalp condition linked to hair loss and mental health issues, with limited treatment options.

Prosopis farcta has strong antioxidants, useful for food and medicine.

Recognizing IPPP is crucial to prevent misdiagnosis and unnecessary treatments.

Cashmere quality differences are due to gene expression variations affecting hair development and adaptation to cold.

Phosphatidylinositol 4-kinases are crucial for root growth, defense, and immunity in Arabidopsis thaliana.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Significant progress was made in understanding PXE, but effective treatments are still needed.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

Only 5 duku seedlings showed resistance to stem canker, linked to specific mother tree traits.

Pregnancy right after giving birth in mice lacking IL-10 causes milk that leads to liver issues and hair loss in their babies.

Defective repair processes may cause immune activation and inflammation in psoriatic disease.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

Lichen planopilaris can be triggered by prolonged scalp traction and can be treated with corticosteroids.

Stroma structural changes cause large pores and skin laxity, regardless of age or ethnicity.

A rare hair disorder with multiple hairs from one follicle was found on a patient's abdomen.