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Patients at dermatology specialist hospitals had lower death and readmission rates but higher treatment costs.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

A man developed skin lesions as a side effect of a gamma secretase inhibitor used for treating a tumor.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

Interface dermatitis is the most common skin change in drug-induced hypersensitivity syndrome.

Five existing drugs may help fight Swine Acute Diarrhea Syndrome Coronavirus.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

HHV-6 reactivation may be linked to psychiatric disorders and can improve with antiviral treatment.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Blocking a specific enzyme can reduce the negative impact of stress hormones on hair growth cells.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Most female students in Aden, Yemen, have low vitamin D levels, causing health issues.

SVF-enhanced adipose transplantation shows potential as a hair loss treatment.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

A new DSG4 gene mutation causes hair defects in a young girl.

The modified stem cells with VEGF165 in a special scaffold improved blood vessel growth and wound healing for skin repair.

Growth hormone therapy can improve symptoms and growth in children with Vitamin-D Dependent Rickets Type-2.

Hepatitis B vaccination can trigger HSP, and vitamin D correction and tonsillectomy can effectively manage it.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.