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

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Different genes are linked to various types of hair loss.

Sox6 is important in heart and kidney health, affecting diseases like diabetes, heart disease, and high blood pressure.

Correct diagnosis and treatment are crucial for effective management of lipid storage myopathies.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Patients often experience long-lasting changes to their hair after stem cell transplants.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Fat tissue stem cells may help increase hair growth.

Certain fats in the skin help control inflammation and health, and changing these fats through diet or supplements might treat skin inflammation.

Many elderly women experience unwanted facial hair and various hair loss conditions, with treatments available for each condition.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

Correcting nutrient deficiencies may help with hair loss, but the benefits of supplements without a deficiency are uncertain and could be harmful.

Janus kinase inhibitors are promising drugs for treating autoimmune and inflammatory diseases.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.

5-alpha-reductase inhibitors may cause a low incidence of erectile dysfunction that decreases over time.

A man experienced hair loss from radiotherapy, which can be temporary or permanent depending on radiation dose, with potential treatments available.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

Proper antifungal treatment is crucial to avoid misdiagnosis and prevent scarring alopecia.

Inducing ferroptosis in hepatic stellate cells is crucial for treating liver fibrosis.