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An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

FPHL is a common, age-related, genetic hair loss with unclear causes and limited treatment options.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Some supplements may help with hair loss, but there's not enough strong evidence to recommend them without doctor advice.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Aromatase gene variation may increase female hair loss risk.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

The conclusion is that proper evaluation and treatment of hair loss in midlife women is important, considering the emotional impact and potential for various treatments.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

PCOS may have evolved as an advantage in past environments with food scarcity.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Hair loss in women can be slowed with treatment, but more research needed for better solutions.