Search

everythinglearnresearchcommunity

for

Search:↓

A Korean girl developed kinky hair without known cause or effective treatment.

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

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Patients with acanthosis nigricans often have insulin resistance and signs of increased male hormones, but treatment targeting these male hormones is generally ineffective.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Telogen Effluvium is a condition causing excessive hair loss due to stress, illness, drugs, or hormonal changes, and can be treated with specific products or naturally resolves after 3-4 years.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

The document discusses how to identify and manage common skin conditions in children.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

The document concludes that diagnosing female hair loss requires careful examination, with treatments varying by condition and psychological support often necessary.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

Tofacitinib may slow hair loss in scarring alopecias but is unlikely to regrow significant hair.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Deep learning can accurately detect Alopecia Areata with up to 98.3% accuracy.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

PPAR agonists show promise for skin conditions but need more research before being a main treatment.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Some patients experience temporary hair loss after ulcerative colitis surgery, likely due to illness rather than the surgery itself, and it usually grows back within six months.

The Hair India 2010 conference introduced a new hair loss classification and highlighted advanced diagnostic techniques in trichology.

Doctors should know how to diagnose and treat PCOS, which often involves checking for high male hormone levels and using medications to manage symptoms.

Understanding causes and treatments helps doctors manage hair loss effectively.

Valproic acid can cause hair loss when taken orally but may promote hair growth when applied topically.