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EZH2 levels decrease as fetuses develop and are higher in adult skin, which may affect skin growth and repair.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

MOF controls skin development by regulating genes for mitochondria and cilia.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Hormonal contraceptives are effective for teens but require careful consideration of side effects and individual health.

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

Hair follicle biology advancements may lead to better hair growth disorder treatments.

CDP is crucial for lung and hair follicle cell development.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

The circadian clock is crucial for tissue renewal and regeneration, affecting stem cell functions and having implications for health and disease.

Biotin treatment can significantly improve hair loss and motor functions in certain metabolic disorders.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

The document concludes that the skin's immune system is complex, involving interactions with hair follicles, nerves, and microbes, and can protect or cause disease, offering targets for new treatments.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

Metformin should be used for PCOS mainly in those with glucose intolerance, and has limited benefits for infertility or hirsutism.

Not enough vitamin B6 in pregnant rats' diets caused poor development and health in their babies.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Hair follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

Shrunken heads retain some facial features and hair characteristics, allowing for limited individual identification.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Operative hysteroscopy is still the main treatment for Asherman syndrome, but more research is needed on post-surgery methods.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Treating PCOS is complex, involving medication like metformin and lifestyle changes, and requires attention to mental health due to high depression and anxiety rates.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.