Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Recognizing lupus as a cause of severe gut issues is crucial for effective treatment.

Pulsed dye laser treatment was effective for a skin condition resistant to other treatments.

Early diagnosis, genetic testing, and personalized care are essential for managing tuberous sclerosis.

An elderly woman's swollen, painful foot was found to be caused by a rare type of bone lymphoma, which improved with radiation treatment.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Scalp lesions in discoid lupus are more common in women and linked to other autoimmune diseases.

The LMNA mutation affects skin structure even in asymptomatic carriers.

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

Collagen CLR and placenta extract may help treat diffuse hair loss.

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

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

Early diagnosis of Bloch-Sulzberger Syndrome is crucial to prevent severe complications.

Hair loss in lupus is different from hair loss in alopecia areata and may indicate lupus activity.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

Antiphospholipid syndrome can severely damage adrenal glands, requiring early diagnosis and treatment.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A patient with Sézary syndrome showed improvement after treatment and the study suggested follicular mucinosis might indicate future lymphoma risk.

CCCA mainly affects Black women and is linked to high-tension hairstyles, heating tools, chemical relaxants, and genetics.

Children with chilblain-like lesions may have a link to COVID-19.

Bcl-2 helps hair regeneration but can also increase cancer risk.

GLI and EGF signalling affect Basal Cell Carcinoma development and could be therapeutic targets.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.