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Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

The research gives new understanding on how human steroid 5α-reductases work and how drugs like finasteride inhibit them, which could help in creating new drugs.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Keratin from human hair helps nerves heal faster.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

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

Cross-sex hormone treatment in transsexual individuals helps understand how sex hormones affect diseases like heart disease and diabetes.

Male pattern baldness may be caused by scalp pressure on hair follicles, which increases with age and leads to a cycle of hair loss. This process is not directly determined by genes.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Chaga mushrooms contain compounds that may promote hair growth better than common treatments.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

A cat had a rare fungal infection caused by Microsporum gypseum.

Oxidative stress and immune dysfunction are linked to both Hashimoto's thyroiditis and polycystic ovary syndrome, with diet and specific treatments important for managing these conditions.

High doses of Lepidium sativum seed extract are toxic and should be used with caution.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

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

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

A child with a rare vitamin D-resistant condition improved with treatment.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.