Search

everythinglearnresearchcommunity

for

Search:↓

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

Patients with pernio have lower vitamin B12 and ferritin levels than healthy people.

Vitamin D deficiency is common in people with certain types of hair loss, like alopecia areata and female pattern hair loss.

Biotinidase deficiency can be easily diagnosed and treated with biotin to prevent serious harm.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A woman's hair loss worsened after starting hepatitis C treatment due to immune changes in her hair follicles.

Calcitriol-resistant rickets is an inherited disorder that affects hair growth and causes hair loss.

PNH can occur in patients with SLE, so doctors should be aware of this.

Lowering homocyst(e)ine levels can reverse skin and hair lightening by restoring enzyme activity needed for pigmentation.

Low serum ferritin levels are linked to more severe and longer-lasting alopecia areata in children.

Lower adiponectin and higher leptin levels may predict hair loss in alopecia areata.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Valproic acid can rarely cause reversible nail discoloration.

Zinc supplements effectively treat acrodermatitis enteropathica.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Alopecia Areata may involve reduced antioxidant defenses in hair follicles, affecting stem cell function.

People with Alopecia Areata are more likely to have certain health issues like ulcerative colitis and type 1 diabetes, but less likely to have others like hypertension and type 2 diabetes.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Anorexia nervosa may cause a hair defect called pili torti due to malnutrition and high vitamin A levels.

The treatment was not recommended due to limited effectiveness and significant side effects.

Zinc supplements effectively treat inherited zinc deficiency in infants.

A patient with Crohn's disease grew back their hair after stopping Adalimumab, which had caused hair loss.

Children with alopecia areata should only have thyroid screening if they have Down syndrome, a history of atopy, family history of thyroid disease, or signs of thyroid problems.

A patient with zinc depletion improved after zinc supplementation during parenteral nutrition.

Child with rickets improved with a specific vitamin D therapy, but alopecia did not change.

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

Mitochondrial stress can lead to atopic dermatitis.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.