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Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Vitamin C supplementation can resolve pulmonary arterial hypertension caused by vitamin C deficiency.

Hematopoietic stem cell transplantation does not significantly affect COVID-19 severity in children with immune disorders.

A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

Generalized hair follicle hamartoma can occur with systemic lupus erythematosus.

Selenium deficiency caused symptoms in a child, which improved with selenium supplements.

Frontal Fibrosing Alopecia may be linked to autoimmune diseases like Sjögren's syndrome.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Iron infusions can help improve hair loss in patients who can't take oral iron supplements.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

There is no clear link between low serum ferritin and chronic diffuse telogen hair loss.

Sickle cell disease affects BMI and pain frequency, with HbSS patients having more pain and unhealthy BMI.

High blood pressure drugs often cause skin lupus, stopping the drug usually helps. A vaccine helps prevent genital herpes and HPV-16. More frequent light therapy clears psoriasis faster. No link was found between low iron and chronic hair loss.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

The document suggests finding a simpler, cheaper way to diagnose Uncombable Hair Syndrome.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Low androgen levels can still cause female pattern hair loss.

Human hair follicle stem cells can help heal wounds faster.

Iron deficiency is the main cause of hair loss in women, and iron supplements started within 6 months can improve hair health.

Early iron deficiency can lead to anemia during puberty, so it's important to address it early.

Some children who had stem cell transplants developed permanent hair loss, especially when treated with a drug called busulphan.

The gene HDC is important for the development of hair follicles in newborn mice.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Applying linoleic acid to the skin fixed essential fatty acid deficiency symptoms.

Allergic reactions to blood thinners are rare but can be serious, requiring careful testing and alternative treatments.