Search

everythinglearnresearchcommunity

for

Search:↓

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

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.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

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

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Facial plastic surgery has evolved to focus on less invasive techniques and innovative technologies for cosmetic and reconstructive procedures.

The document concludes that improving the appearance of posttraumatic facial scars is possible with careful treatment and realistic expectations.

PlacMA hydrogels from human placenta are versatile and useful for cell culture and tissue engineering.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

The document is a detailed medical reference on skin and genetic disorders.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

The document concludes that proper diagnosis and evidence-based treatments are crucial for managing hair diseases, and psychological support for patients is important.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

Acne not improved by usual treatments may indicate a genetic disorder.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A girl inherited excessive body hair from her mother and grandmother.

Excessive body hair can signal complex health issues.

People with reproductive, thyroid disorders, and type 2 diabetes can experience voice changes, but more research is needed to understand this better.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

The document explains how to identify different hair problems using a microscope.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

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

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.