Search

everythinglearnresearchcommunity

for

Search:↓

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

Finasteride and dutasteride are effective in treating male hair loss but can cause sexual side effects and birth defects.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

A 6-year-old girl's inability to grow her hair long was due to Loose Anagen Hair Syndrome, which causes hair to shed easily and may improve with age.

Hirsutism greatly lowers the quality of life for Turkish women.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Eating more protein during fast weight loss can prevent hair loss.

The document concludes that more research is needed to fully understand the causes of PCOS.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Regular use of sunscreen may be linked to frontal fibrosing alopecia.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Skin symptoms can indicate endocrine disorders and have various treatments.

Polycystic ovary syndrome (PCOS) is a major health issue for women in Egypt, affecting 14% of fertile women and 37.5% of infertile women.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

The document suggests various treatments for PCOS, including medication for menstrual issues, insulin resistance, and excess hair, as well as fertility treatments, while highlighting the need for personalized care and lifestyle changes.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.