Search

everythinglearnresearchcommunity

for

Search:↓

Lupus nephritis patients face more challenges in family planning, work, symptoms, medication, and quality of life than those without it.

A rare biotin deficiency in an Iraqi family caused severe symptoms but was successfully treated with lifelong biotin.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

Balding in men is strongly linked to high blood pressure and family history.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Most women with polycystic ovary syndrome were first diagnosed by their family doctor, who may need to record symptoms better and rely less on ultrasounds.

PCOS and related metabolic issues often run in families.

Monilethrix causes different levels of hair loss in family members.

Older age, family history, and low iron levels increase the risk of female hair loss.

A 24-month-old Nigerian girl developed early puberty with no family history, needing treatment her family couldn't afford.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.

Androgenic alopecia in men is mainly linked to family history, hormonal imbalances, and metabolic issues, but can also be influenced by lifestyle habits, environmental factors, and deficiencies in certain vitamins and microelements like copper.

Hair loss in twins may be linked to family history of hair loss, high blood pressure, heart disease, and possibly anxiety, but more research is needed.

Women with PCOS may take longer to get pregnant but can have a normal family size, and should manage their overall health to reduce long-term health risks.

Hair loss in middle-aged women is often linked to insulin resistance and a family history of hair loss, particularly from their fathers.

Activins and follistatins, part of the TGFβ family, are crucial for hair follicle development and skin health, affecting growth, repair, and the hair cycle.

Teen hair loss common in boys, linked to family history and mild symptoms.

A new mutation in the HR gene causes hair loss in a specific family.

Oxidative stress increases in early hair loss, and family history plays a role; antioxidants may help future treatments.

Pediatric androgenetic alopecia is linked to obesity, family history, hormonal imbalances, and requires personalized treatment including managing comorbidities.

Older age, higher BMI, and family history of diabetes increase the risk of gestational diabetes in pregnant women.

Alopecia areata was most common in people in their 30s and 40s, with some family history and a higher relapse rate, and larger bald areas responded better to specific immunotherapy.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Most vitiligo patients in Makkah are young women, often with family history and thyroid issues.

Early hair loss common in Chinese males, linked to family history and smoking; early treatment advised.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.