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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Women generally handle heart enlargement better than men, but it's riskier for them if it occurs; hormones like estrogen offer some protection.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

The conclusion is that certain cell interactions and signals are crucial for hair growth and regeneration.

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

Platycarya strobilacea extract is a strong antioxidant that can grow hair better than minoxidil.

The document concludes that understanding how adult stem and progenitor cells move is crucial for tissue repair and developing cell therapies.

Understanding the mouse hair cycle is crucial for cancer research.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Exposure to finasteride in the womb caused lasting reproductive issues in male rats.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Extracellular vesicles may effectively treat hair loss with minimal side effects.

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

Benign Prostatic Hyperplasia may be caused by changes in how the body processes male hormones.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

No treatment fully prevents hair loss from chemotherapy yet.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Not enough vitamin B6 in pregnant rats' diets caused poor development and health in their babies.

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.

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

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

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.