Search

everythinglearnresearchcommunity

for

Search:↓

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Early recognition and treatment of VATS in transplant patients improve outcomes.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

CCCA is a scarring hair loss condition mainly in African descent women, possibly caused by genetics and hairstyling, treated with gentle hair care and medications.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

Avacopan may cause unexpected side effects, so early monitoring is important.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Sympathetic activation and venous tone are crucial for heart failure symptoms.

ADSC-CE treatment safely increases hair density and thickness in androgenetic alopecia patients.

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

Most patients with Central Centrifugal Cicatricial Alopecia at the reviewed institution were middle-aged Black women, often with no symptoms, and commonly treated with topical medications.

The woman was diagnosed with Vogt–Koyanagi–Harada disease and successfully treated with medication, restoring her vision and stopping headaches.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Detecting early breast arterial calcifications can help assess cardiovascular disease risk.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

Early intervention is important for limited systemic sclerosis patients due to higher pain and ulceration risks.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Primary essential CVG is a rare, benign scalp condition with treatment focusing on symptom management and hygiene.

Fat tissue-derived cells show promise for repairing body tissues, but more research and regulation are needed for safe use.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

VESALT improves alopecia areata assessment by including non-scalp areas and is reliable and user-friendly.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.