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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The dog died from myxedema coma linked to severe atherosclerosis and thyroid issues.

Untreated Sheehan's Syndrome caused severe heart failure in a woman, which improved with hormone and heart failure treatment.

The document does not determine if adults with aphallia are fertile.

Aggressive SLE treatment helped hair regrowth and improved oral plaque, but scalp lesions stayed.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

The patient recovered well and returned to college without any lasting issues.

Hair loss may indicate higher risk of heart disease.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

Onychomatricoma is a unique nail tumor that mimics the entire nail unit and is not related to other hair-related tumors.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

Onyx® embolization effectively treats facial arteriovenous malformations with minimal complications.

Granulomatous Alopecia Areata is rare and may be caused by hair antigens or follicle destruction.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

A woman with non-classic CAH had unusual heavy periods and high hormone levels, improved with treatment.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Pilomatricoma is a rare, benign skin tumor that requires surgical removal for best results.

Alopecia areata patients have a higher risk of subclinical atherosclerosis, and carotid ultrasound can help assess their cardiovascular risk.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Alopecia areata may be linked to changes in body fat but not to heart or artery issues.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.