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A genetic defect in vitamin D receptors causes severe rickets and hair loss in children, but some heal as they age.

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

A leukemia patient showed skin peeling similar to kwashiorkor, a severe protein deficiency.

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

The boy's scurvy symptoms improved with vitamin C treatment, highlighting the need for a balanced diet.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

A patient developed hair loss after hepatitis C treatment with sofosbuvir and ribavirin.

Older age, pre-existing skin conditions, cirrhosis, and pegylated interferon use increase the risk of skin issues during hepatitis C treatment.

The document concludes that early diagnosis of Balint's syndrome is crucial for effective treatment and that understanding drug interactions, like between ritonavir and statins, is important for patient care.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Children taking higher doses of valproic acid had lower biotinidase activity, which may lead to biotin deficiency, but biotin supplements could help.

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

Fosravuconazole effectively treated a woman's scalp infection without side effects.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Vitamin B12 deficiency can cause skin and hair color changes, which are reversible with treatment.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

A man's skin condition and poor diet led to a scurvy diagnosis.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A girl had rickets due to a gene mutation affecting vitamin D response.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Specialized ribosomes affect aging in human skin cells.

Retinoic acid is not linked to hair loss from fluconazole use.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

A woman lost all her body hair after hepatitis C treatment, but it started to grow back a year after stopping the treatment.

The boy's symptoms improved with vitamin C treatment, highlighting the need to consider scurvy in kids with unusual diets.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.