Search

everythinglearnresearchcommunity

for

Search:↓

Leontopodium alpinum extract may help reduce hair shedding by keeping hair in the growth phase longer.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

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

The definition of Polycystic Ovary Syndrome may change with new research, and careful screening is key for managing the condition.

Fatty acid transport protein 4 is essential for skin and hair development.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

Genes and hormones cause hair loss, with four genes contributing equally.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

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

Premature graying of hair may suggest health issues and currently lacks effective treatments.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

5-alpha reductase deficiency leads to male sexual development issues and treatments like finasteride help with prostate enlargement and hair loss.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

IGF-1 may affect hair growth and loss, but more research is needed to confirm effective and safe treatments.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Looking at skin can help find and treat serious diseases early.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Curcumin and its derivatives can block an enzyme important for making testosterone, with one derivative being particularly strong.