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The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Some COVID-19 pneumonia patients in Veracruz, Mexico had rare skin issues like temporary hair loss linked to disease severity.

Repurposing existing drugs for COVID-19 shows promise but requires more research to confirm effectiveness.

Ixekizumab has known and some unexpected side effects.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

A skin rash after the AstraZeneca COVID-19 vaccine was treated successfully with medication.

Booster doses of Covaxin improve protection against the Omicron variant.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

A woman got a serious strep infection from an IUD, likely passed from her husband's infected throat during sexual activity.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Danoprevir, remdesivir, and saridegib may effectively inhibit SARS-CoV-2.

RHUPUS should be considered in children with deforming arthritis.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

The AndroCoV Clinical Scoring is an accurate, easy, and free way to diagnose COVID-19 without a lab test.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Most children with MIS-C showed significant improvement by 6 months.

Eosinophilic pustular folliculitis should be considered in teens with persistent skin issues for accurate diagnosis and treatment.

Epidermal nevi are skin cell clusters linked to various syndromes.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

Cannabidivarin (CBDV) may help brain cell growth and survival through the TRPV1 receptor.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Diabetic ketoacidosis is common among people with Type 1 diabetes in Makkah Al-Mukarramah City.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

Early recognition and treatment of SLE can improve outcomes in patients with complex symptoms.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.