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Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Dutasteride effectively treats benign prostatic obstruction, improves urinary flow, reduces prostate size, and may prevent prostate cancer, but can cause sexual side effects.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Medical treatments like chemotherapy and radiotherapy can harm sperm production, so freezing sperm before treatment is important for men who want children later.

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.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

No link between hair loss and blood groups or Rhesus factor.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Hair loss in women, often not related to male hormones, increases with age and can cause significant emotional distress.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

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.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

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.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

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

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

The 14-3-3σ gene is essential for preventing hair loss.

Overexpression of HDGF in melanocytes does not cause cancer.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Minoxidil improved hair growth in a child with a rare genetic disorder.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Vitamin D receptor is crucial for bone health and mineral metabolism.

Blocking the ATX-LPA pathway may improve insulin sensitivity and mitochondrial function in obesity.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.