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A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Women with Systemic Lupus Erythematosus should have closely monitored pregnancies and avoid certain medications to improve their pregnancy outcomes.

Some skin diseases and their treatments can negatively affect male fertility.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Early treatment of acne is crucial to prevent scarring and psychological effects.

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

The book is highly praised as an essential resource for plastic surgeons, despite minor gaps.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

Beauty is subjective and culturally variable, but certain facial features like symmetry are universally recognized as attractive.

Some cosmetics and dermatological drugs can cause allergic reactions and side effects, like skin irritation and systemic issues.

The document covers all aspects of plastic and reconstructive surgery, from basic techniques to specific procedures for various body parts.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

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

Facial contouring is crucial for the satisfaction and well-being of Chinese transgender females.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

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.

Using animal names for skin conditions helps with learning and memory.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

The document explains the genetic causes and characteristics of inherited hair disorders.

Woolly hair is a rare genetic condition with no effective treatments.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.