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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

A mushroom extract might reduce hair loss and liver damage caused by certain chemotherapy drugs in animals.

Thallium exposure can cause serious health issues, including nerve damage and hair loss.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Finasteride treatment in male rats can reduce fertility and affect sperm development in their offspring.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

ADSC-derived extracellular vesicles show promise for skin and hair regeneration and wound healing.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A hair tightly wrapped around a toddler's toe caused severe crying and was treated by surgery.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

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

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

A man from Brazil had a rare case of leprosy on his scalp, which improved with treatment.

The document reviews patents on nanoparticle systems used to deliver drugs, discussing their creation, use in treatments, and commercial applications.

Microsponges delivery system is a safe, versatile method for controlled drug release in various treatments.

Biotin, alone or with minoxidil, effectively treats short anagen syndrome.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A toddler's chronic finger ulcer was successfully treated after removing a hair causing hair-thread tourniquet syndrome.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Endoscopy-assisted surgery for craniosynostosis showed excellent outcomes with minimal complications and most patients went home the day after surgery.

A 17-year-old girl had severe, on-and-off hair loss, likely due to COVID-19. She was treated with Vitamin D3, biotin, and other supplements, and saw some improvement within a month.

Ovarian hemangioma is a rare, benign tumor that can be treated effectively with surgical removal.

An 11-year-old girl with compulsive hair pulling was successfully treated with therapy and medication.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Children's screen time increased during the pandemic, causing various health issues.

A toddler who accidentally swallowed hair growth medicine experienced serious heart-related side effects but recovered after hospital treatment.

Hair loss is more common in male Chinese college freshmen, and it's linked with rosacea but doesn't affect their quality of life.

Female pattern hair loss is more common in rural areas among secondary school girls.