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

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

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Skin cysts might help advance stem cell treatments to repair skin.

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.

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.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

The document concludes that treating skin conditions should include psychological care and a multidisciplinary approach is essential for effective management.

The document announced plastic surgery events and courses for late 1997.

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

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

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.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

PCOS affects women's health by increasing the risk of diabetes, heart disease, and reproductive issues.

Scientists found a gene in mice that causes early hearing loss.

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

New understanding of the causes of primary cicatricial alopecia has led to better diagnosis and potential new treatments.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

The conclusion is that primary scarring alopecia is a complex condition that requires early and accurate diagnosis for effective treatment.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

The monkey's hair loss was due to an autoimmune disease, not genetics.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

Mechanical forces are crucial for shaping cells and forming tissues during development.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

New DNA analysis and machine learning are advancing forensic science, improving accuracy and expanding into non-human applications.

The right amount of retinoic acid is essential for normal hair growth and development.