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PRP injection for hair growth can cause reversible vision loss due to inflammatory optic neuropathy.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

Looser dietary restrictions can improve growth and reduce illness in methylmalonic acidemia patients.

The treatment with valproate, acetylcarnitine, folic acid, and vitamin B12 may improve muscle strength in children with SMA without significant side effects.

Early diagnosis of leprosy is crucial to prevent disabilities and spread, even in non-endemic areas.

Alopecia areata can be an early sign of Hodgkin’s lymphoma and may improve with lymphoma treatment.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Managing myasthenia gravis is crucial and does not worsen primary Sjögren's syndrome.

IT PEP may help recovery after spinal cord injury, but more research is needed.

Manganese levels in hair may be linked to multiple sclerosis.

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

Memantine may slightly improve memory in people with Down syndrome, but more research is needed.

Mitochondrial dysfunction is linked to various skin conditions and could be a target for treatments.

SLHA can be hard to diagnose and needs teamwork between specialists.

A girl with no hair neglect developed plica neuropathica in the hospital, lost all her hair, but it grew back.

Some children with methylmalonic and propionic acidaemias have skin problems related to their condition and diet.

Recognizing myxedema coma is crucial due to its high risk and unusual symptoms.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Topical 5-Fluorouracil can rarely cause nerve damage, especially in people with a certain genetic deficiency.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

Mesenchymal stem cells are effective and safe for treating various diseases in children.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

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

Removing a tumor may resolve associated skin and hair symptoms.

New mutations in the DSG4 gene cause a rare hair condition.

PRP injections improve skin appearance and are safe for treating morphea.