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Psychosis can be an early sign of neuropsychiatric lupus, treatable with tailored medication.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

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.

The virus was not found in the semen and urine of a man who tested positive for COVID-19.

Iron deficiency may contribute to hair loss.

The research found that MRI and certain hormone levels can help tell apart ovarian tumors from hyperthecosis in postmenopausal women, but tissue analysis is still needed for a definite diagnosis.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

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

FGF18 treatment during hair's resting phase can protect against hair loss from radiation.

Lower LDL-c levels predict higher COVID-19 mortality.

A woman had a rare, non-cancerous skin growth on her face, which was removed and did not come back after a year.

The OVOL1-OVOL2 axis is important for hair follicle differentiation and can help diagnose certain hair-related tumors.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Oestrogens are key for bone growth during puberty in both boys and girls.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Sorafenib after liver surgery may increase survival for some liver cancer patients.

Taking Propecia might lead to the development of cataracts.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

A woman with high testosterone and an adrenal nodule had an ovarian tumor causing her symptoms, which improved after the tumor was removed.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Blood tests can detect ovarian Leydig cell tumors when scans don't, and surgery can confirm and treat these tumors.

Insulin resistance is linked to larger thyroid volume in patients with polycystic ovary syndrome.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Rind-based techniques can lower scalp radiation dose and reduce hair loss in brain cancer treatment.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

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

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.