Search

everythinglearnresearchcommunity

for

Search:↓

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Testosterone and its metabolites affect brain functions and could help treat neurological disorders.

Sodium selenate was found to be safe and possibly slows Alzheimer's progression, but more research is needed.

Minoxidil use during pregnancy may cause fetal harm.

Early diagnosis and proper treatment improve outcomes for methylmalonic acidemia.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

The document concludes that managing side effects of MS therapies is crucial for treatment success and patient adherence.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Creatine monohydrate is safe and effective for muscle recovery and performance, especially for those with low creatine levels.

Zinc helps reduce the severity of depression.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Modified PRP therapy successfully treated severe alopecia unresponsive to traditional methods.

Papulopustular rosacea is an inflammatory skin condition treatable with lifestyle changes and medications.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

Bombax ceiba stem bark extracts can lower blood pressure, but high doses can be toxic and lethal.

The document concludes that transsexual individuals often experience improved quality of life after transitioning, despite higher risks of psychiatric issues and mortality.

Finasteride for hair loss can cause long-lasting sexual side effects like low libido and erectile dysfunction.

Methotrexate treats various disorders by inhibiting DNA synthesis, but careful monitoring is needed to avoid toxicity and manage side effects.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

New research on prostamide F2α has led to treatments for glaucoma and eyelash growth and may have more medical uses.

The model and estimator can predict drug exposure in kidney transplant patients well.