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BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Some conditions mimic PCOS symptoms and need careful diagnosis to treat potentially serious health issues.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Prenatally androgenized ewes can model increased hair diameter in women with PCOS.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Glucocorticoids are powerful anti-inflammatory drugs that must be used carefully to avoid serious side effects.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

People in Jeddah know about Vitamin D and its sources but are unclear on how much they need daily, and while many women take supplements, attitudes towards increasing Vitamin D levels vary.

Early detection and comprehensive treatment of PCOS are crucial due to its long-term health impacts and associated risks.

Physical activity, height, and smoking affect prostate cancer risk.

A new gene mutation causes insulin resistance in a girl and her mother.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Multimodal recruitment effectively gathered a diverse group for an online survey on ovulation and menstruation health.

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

Beta-blockers and anti-anginal medications have various side effects and interactions that require careful monitoring and individualized treatment.

Bariatric surgery can cause serious mineral deficiencies, requiring better patient education and monitoring.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

High hair cortisol levels indicate stress in cows due to poor shelter conditions and health issues.

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

A new method accurately detects bisphenols and parabens in human hair.

Alopecia areata causes a significant economic burden in Japan, mainly due to productivity loss.

Hair loss peaks in spring and regrowth in late summer, with pregnant females losing the most hair.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

The KRTAP21-2 gene affects wool length and quality in sheep.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.