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hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Knuckle darkening can be an early sign of vitamin B12 deficiency.

A gluten-free diet resolved a girl's symptoms, revealing undiagnosed Coeliac disease as the cause.

A 15-year-old boy's skin and hair condition worsened due to improper treatment, leading to severe health issues.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Oxidative stress is higher in women with PCOS, especially if they're obese, and it may increase their risk of heart disease.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Micronutrient deficiencies may cause hair loss in people on long-term parenteral nutrition.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.

Men with advanced liver disease and high oestrone and low testosterone levels have worse health outcomes.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

The levels of zinc, vitamin D, ferritin, and selenium are different in people with androgenic alopecia compared to a control group.

Hair loss is linked to eating less soy, having lower blood vanadium, and a specific genetic variation in Taiwanese communities.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

Routine thyroid tests for diffuse alopecia in women may not be necessary, but checking for iron deficiency anemia could be useful.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Relatives of women with PCOS symptoms are more likely to have similar health issues.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Low ferritin levels are linked to chronic hair loss in women.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Chinese women with PCOS and a BMI of 24 or higher should be screened for fatty liver disease.