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A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Sweet syndrome can be the only sign of hairy cell leukemia relapse.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

The twins' condition is unique and doesn't match any known syndromes.

Lambs fed a liquid diet showed abnormal wool and skin, which improved with more B-vitamins, suggesting a link to B-vitamin deficiency.

Canine leishmaniasis is present in Oklahoma, USA.

Björnstad syndrome causes twisted hair from birth.

Keratosis pilaris significantly affects quality of life and shows specific skin changes.

Yorkshire Terriers with Colour Dilution Alopecia have reduced melanin and hair structure issues.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Selenium deficiency can cause skin and hair color loss, muscle weakness, and blood cell changes, but these improve with selenium supplements.

A cat with sebaceous adenitis improved after treatment with shampoo, ciclosporin, and fatty acids.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

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

Canine pemphigus foliaceus involves significant immune activity and shares similarities with human pemphigus.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Keratin mutations may cause scarring alopecia by damaging hair structure.

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

Camels in South Iraq were cured of skin infections with antibiotics and supplements.

Propylthiouracil, a thyroid medication, can cause skin blood clots and immune-related blood vessel inflammation.

A girl inherited excessive body hair from her mother and grandmother.

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

Illegal wildlife captivity poses health risks and highlights the need for conservation and public health awareness.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

A rare scalp condition called Erosive pustular dermatosis is hard to diagnose and treat.