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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 patient developed nerve problems as a side effect of a hair loss treatment called tofacitinib.

Long-haul COVID can cause lasting symptoms affecting many body systems and may be linked to ongoing inflammation and immune system issues.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

COVID-19 vaccination may be linked to MIS-C in children, highlighting the need for quick diagnosis and treatment.

Long COVID causes a wide range of long-lasting symptoms that change over time and are hard to diagnose and treat.

Certain vitamins in wrong amounts, alcohol abuse, metals, and other toxins can cause serious brain and nerve damage.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Epilepsy and certain epilepsy drugs can lead to reproductive problems in women, but changing medication might improve these issues.

Tight hairstyles can cause a rare scalp condition with thick skin folds.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Syphilis can cause hair loss and treating the infection can reverse it.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.

Mood stabilizers like lithium and anticonvulsants have side effects that can lead to patients stopping their medication, and managing these effects is important for treatment adherence.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Levetiracetam is widely used and generally well-tolerated for treating idiopathic generalized epilepsies, with tiredness as the main side effect.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Existing drug dexamethasone may lower death risk in severe COVID-19 cases; more research needed for other drugs.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Stress worsens Tourette symptoms by increasing allopregnanolone levels.

Some skin disorders might be linked to H. pylori infection, but more research is needed to confirm this.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Vitamin B12 deficiency can cause skin darkening and increased blood vessels, but treatment can improve symptoms.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.