Search

everythinglearnresearchcommunity

for

Search:↓

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

5% minoxidil can significantly increase hair growth in TRPS patients.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

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

The document explains the genetic causes and characteristics of inherited hair disorders.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

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

Hair transplantation successfully treated hair loss in a patient with Trichorhinophalangeal syndrome.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

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

Melanocytes are diverse cells important for pigmentation and skin health, influenced by genetics and environment.

The microenvironment, especially mechanical forces, plays a crucial role in hair growth and could lead to new treatments for hair loss.

Bio-pulsed stimulation increases production of beneficial vesicles from bird stem cells that improve skin and hair cell functions.

Different hair loss types need accurate diagnosis for proper treatment.

Bioassays help find useful compounds in nature for making medicines, supplements, and cosmetics.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Minoxidil improved hair growth in a child with a rare genetic disorder.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Different ligands change the shape of the TRPV3 ion channel in unique ways.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.