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The flap advancement technique effectively treats severe scalp skin conditions, preserving hair and improving appearance.

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

Iron deficiency might contribute to hair loss in women.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.

Male mice are more susceptible to autism-like changes from valproic acid than female mice.

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

Turkish women with hirsutism experience lower quality of life, especially those with PCOS, regardless of hair growth severity.

5α-reductase inhibitors can cause sexual problems, higher risk of aggressive prostate cancer, and depression.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

An 8-year-old girl with Rapunzel syndrome had a hairball removed from her stomach and intestines and recovered well after surgery.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Advances in genetics may lead to targeted treatments for hair disorders.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

Skin issues can indicate immune system problems.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

The meeting covered new findings in children's skin conditions and treatments, including the benefits of super absorbent polymer diapers.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

The twins' condition is unique and doesn't match any known syndromes.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

People with Down's syndrome are more likely to have syringomas.

The document concludes that HAIR-AN syndrome should be considered when a patient shows severe hyperandrogenism and insulin resistance after excluding tumors.

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