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Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Alopecic and aseptic nodules of the scalp are rare, treatable, and often resolve with doxycycline or on their own.

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

A woman's excessive hair growth was caused by a rare benign tumor in her adrenal gland, which was successfully removed.

Favus, a rare fungal infection, has reappeared in Japan.

Taking 1 mg of finasteride daily could potentially treat rare hair conditions like Acquired Progressive Kinking of the Hair and whisker hair.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Tofacitinib successfully treated a woman's severe symptoms from a rare autoimmune condition.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

The author now believes tricholemmal carcinoma is a rare type of infundibular squamous cell carcinoma and more research is needed on these tumors.

Hair loss can be a key sign of a rare type of rickets when vitamin D treatment doesn't work and advanced tests aren't available.

An 8-year-old boy recovered from a rare case of penile tourniquet syndrome after hair removal surgery.

Elkonyxis, a rare nail condition, improved when patients stopped their nail-picking habits.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

Two dogs in Korea were diagnosed with a rare skin condition usually seen in cats.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Hormonal imbalances in Polycystic Ovarian Syndrome (PCOS) might trigger a rare skin disorder called Confluent and Reticulated Papillomatosis (CRP), so dermatologists should consider checking for PCOS in CRP patients.

Erosive pustular dermatosis of the scalp is a rare condition that causes scarring hair loss, mainly in older women, and requires ongoing treatment.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Low-dose oral minoxidil for hair loss seems to have rare side effects, but more research is needed to confirm its safety.