Search

everythinglearnresearchcommunity

for

Search:↓

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

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

Metabolic syndrome is more common in people with early-onset androgenic alopecia.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

The FDA did not approve certain drugs for prostate cancer prevention due to concerns about their effectiveness and potential risks.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

Sex hormones affect liver fat and metabolic health differently in men and women.

Early balding in young Indian men may indicate a higher risk of metabolic syndrome and potential heart disease.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

A thorough diagnostic process and teamwork are crucial for managing complex hyperandrogenism in postmenopausal women.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.

A potential link exists between unexplained hormone deficiency, hair loss, and testicular tumors, suggesting thorough screening is needed.

Monilethrix causes brittle hair and hair loss, and it runs in families.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Hair loss and metabolic syndrome are linked, sharing causes and treatment options.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.