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A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Trichoscopy can help diagnose Vitamin B12, Vitamin D3, and ferritin deficiencies without blood tests.

Unexplained anemia in older men may be linked to urological issues like urinary retention.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

Gorillas in Gabon improved after protein supplements were added to their diet.

Low ferritin and zinc levels, as well as anemia, are linked to more severe hair loss in Egyptian children with chronic hair shedding.

People need different amounts of biotin based on age and it's important for health, with many foods providing enough.

Diagnosing and treating monilethrix is challenging when it occurs with other hair disorders.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Iron deficiency is common in kidney transplant patients, and while iron treatment helps, it can cause high red blood cell levels.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

Premature greying in kids can signal health issues like vitamin deficiencies or thyroid problems, which can be treated.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A unique gene mutation was found in a family with monilethrix.

Excessive selenium from supplements can be harmful.

Vitamin D-dependent rickets Type II causes bone problems and hair loss, and doesn't improve with Vitamin D treatment.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A person with thyroid problems had rare, swollen, bald spots on their scalp caused by a condition usually found on the shins.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Giant cells found in some male pattern baldness cases may help diagnose it and suggest hair is mistakenly seen as foreign by the body.

Eyelash loss can be a sign of thyroid problems.

A skin condition called pyodermatitis vegetans was found in a patient with multiple myeloma for the first time.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Micronutrient deficiencies might contribute to alopecia areata.