Search

everythinglearnresearchcommunity

for

Search:↓

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.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Acne is strongly linked to high BMI, hair loss, menstrual issues, family history, and eating too many sweets and fatty foods, but not to excessive hair growth.

Most hair disorder patients at the clinic were young adult males, with alopecia areata being the most common condition.

PCOS and related metabolic issues often run in families.

Hair loss from alopecia areata can sometimes regrow in a pattern similar to androgenetic alopecia.

Minoxidil, a common hair treatment, may cause hair to turn grey or change color, especially with long-term use or if you have a family history of grey hair.

Three genes linked to the development of trichilemmal cysts were found.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

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

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

Finasteride effectively treated hidradenitis suppurativa.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

EF and PXE not closely related.

Short Anagen Syndrome causes persistently short hair and increased shedding, usually improving after puberty.

The document describes skin diseases affecting the outer ear in dogs and cats, their spread to other body parts, and treatment options.

Polycystic Ovary Syndrome (PCOS) is a hormonal disorder in women that can cause infertility and other health issues, and it may be improved by treatments that increase insulin sensitivity.

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.

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

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Caffeine may help hair growth in hereditary hair loss.

Isotretinoin can raise CPK levels, so patients need monitoring, especially before surgery.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

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

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

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

Men with a certain type of hair loss (AGA) have higher bad cholesterol and lower good cholesterol levels, making them more likely to get heart disease.

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