Search

everythinglearnresearchcommunity

for

Search:↓

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 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

Homeopathy may help with hair loss caused by various factors, especially during the pandemic.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

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

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Caffeine may help hair growth in hereditary hair loss.

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Fat stem cell treatment is safe and increases hair density for hair loss, but more research is needed.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Drug approvals slowed in 2Q22, but notable drugs like Amvuttra, Camzyos, and Olumiant were approved.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

hsa_circ_0001079 may help diagnose and treat hair loss.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

The document corrects errors in previous articles, including a reversed term, updated subject weights, hair count data, and reference numbering.

PRP injections can help reduce hair loss in some people with Androgenetic Alopecia.

The rash on the infant indicated a serious underlying condition.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.