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Thymosin β4 helps in cell activities, healing, and organ preservation, and treats hair loss and skin injuries.

Biotin treatment improved hair and skin issues in a child with biotinidase deficiency.

A cancer patient's eyelashes grew excessively without other common side effects after taking the cancer drug erlotinib.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

Orange spots in scalp trichoscopy can help diagnose scalp sarcoidosis.

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

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Tinea faciale can be mistaken for lupus due to similar symptoms.

Erlotinib can cause hair loss as a side effect.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

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

A woman's rare scalp condition worsened after using a specific arthritis medication, suggesting such medications can sometimes trigger or aggravate psoriasis.

Narrowband UVB therapy significantly improved a child's rare skin condition.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Trichoscopy helps accurately diagnose temporal triangular alopecia.

SLE can occur in young males and cause knee pain.

Biotinidase deficiency can cause vision and walking problems in children and can improve with biotin treatment.

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

Hypothyroidism-related skin issues in dogs are most common in older male Labradors, causing hair loss, slow heart rate, and obesity.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A patient with a rare chromosome condition also had a rare type of hair loss.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Early diagnosis and treatment of biotinidase deficiency are crucial to prevent vision problems.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Vitamin D-dependent rickets Type II causes bone problems and hair loss, and doesn't improve with Vitamin D treatment.

A child with rough nails also had hair loss and allergies.