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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.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Hair loss in androgenetic alopecia is caused by genetic factors and androgen excess, and can be treated with combined therapies.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

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

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

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

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

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

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Understanding skin structure and development helps diagnose and treat skin disorders.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

Found new possible treatments for hair loss.

Air pollution (PM10) increases skin inflammation and aging by reducing collagen and may trigger a repair response in skin cells.

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

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Inflammasome proteins can indicate the severity and treatment response of various diseases and injuries.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.