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A specific immune response helps control mite populations on the skin, maintaining healthy hair follicles.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

A woman's severe hirsutism was caused by Leydig cell tumors in her ovaries, which improved after surgery.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Azathioprine can cause severe blood issues and hair loss, needing careful monitoring and possible discontinuation.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Androgens like testosterone affect skin health and can lead to conditions such as acne and hair loss, with various treatments available.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

Insulin resistance is linked to PCOS and can lead to other health issues, but treatments like metformin can help manage symptoms.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Taking calcium may help elderly with osteoporosis, birth control with levonorgestrel doesn't increase heart attack risk, Salmonella can cause arthritis, a national ethics committee is recommended, and sulfasalazine might help with a hair loss condition.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Overexpression of HDGF in melanocytes does not cause cancer.