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Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Psoriasis skin changes are complex and might need several biopsies for a clear diagnosis.

Nails can reveal important health information about skin and body conditions.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Neurotoxins can affect neurotransmitter release and have potential in treating muscle, pain, and cancer conditions, but more research is needed on how they work.

Selumetinib effectively reduces tumor size in many children with neurofibromatosis type 1, but can cause skin and hair issues.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

A new type of nerve cell involved in itch perception was discovered.

Keratin gel may help repair damaged nerves.

Epidermal neural crest stem cells from hair follicles can help repair nerve injuries.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Autoimmune Polyendocrine Syndromes involve specific combinations of endocrine and non-endocrine autoimmune diseases.

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

Naevoid bundle hair is an unusual hair growth pattern where multiple hairs fuse together.

Early diagnosis and treatment of TPP can prevent complications.

An elderly woman's swollen, painful foot was found to be caused by a rare type of bone lymphoma, which improved with radiation treatment.

Monilethrix is linked to a gene cluster on chromosome 12.

Netherton's syndrome may have a familial link and doesn't always include atopy.

Physical inactivity is a primary cause of many human illnesses.

Hair loss can cause scalp discomfort.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

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

Glycine is a key transmitter in rat spinal cord synapses, often alongside GABA.

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

Nail abnormalities in children can indicate deeper health issues.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

Hand-foot-mouth disease may cause nail loss in children.