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A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Some blood-thinning medications can increase the risk of bleeding, and certain factors like genetics and other health conditions affect their safety and effectiveness.

Abortion access should be defended on public health grounds, and medical evaluations are crucial in psychiatric cases to avoid misdiagnosis.

Both books are valuable resources in their fields.

The document reviewed various health-related books, focusing on abortion debates, medical conditions, and effective health communication.

The book details advanced techniques in cosmetic dermatology for experienced surgeons.

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

Beta-blockers and anti-anginal medications have various side effects and interactions that require careful monitoring and individualized treatment.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

The twins' condition is unique and doesn't match any known syndromes.

Certain vitamins in wrong amounts, alcohol abuse, metals, and other toxins can cause serious brain and nerve damage.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Linoleic acid (Vitamin F) can help protect against the harmful effects of acrylamide.

An 11-year-old girl with a hair-pulling disorder had a hairball in her stomach and was treated with medication, therapy, and a team of doctors.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

α-mangostin nanoparticles improved acne with minimal irritation.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Hand and forearm transplants can be successful long-term, but they come with challenges like rejection and side effects from immunosuppression.

Removing certain brain receptors in mice worsens seizure severity and response to treatment during hormone withdrawal.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Using three different drugs together may better treat eye diseases like glaucoma and macular degeneration.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

COVID-19 vaccination may be linked to MIS-C in children, highlighting the need for quick diagnosis and treatment.

A brain-made hormone can protect against memory-related brain damage caused by harmful proteins.