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Gut health affects skin diseases, and probiotics might help.

Exposure to certain metals may worsen attention-related behaviors in adolescents, with stronger effects in females.

PRP helps skin heal, possibly through special cells called telocytes.

Changes in gut bacteria can contribute to the development of Polycystic Ovary Syndrome (PCOS), affecting metabolism, immunity, and causing inflammation. Treatments may involve adjusting these factors.

Dutasteride, usually used for prostate issues and hair loss, could potentially treat Amyotrophic Lateral Sclerosis (ALS) due to its neuroprotective, antioxidant, and anti-inflammatory properties, but more testing is needed.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Arsenic exposure from contaminated water severely damages the skin, causing hair loss, pigmentation changes, irritation, and can lead to skin cancer.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Environmental factors and chemicals might affect hormone balance and contribute to common hair loss.

American men are older, more obese, and have longer infertility than Canadian men.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Stress can worsen skin conditions by affecting hormone levels and immune response.

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

Polycystic Ovary Syndrome (PCOS) is a common but often undiagnosed disorder in women that can cause irregular periods, infertility, and other symptoms, and can be managed with lifestyle changes, medication, and sometimes surgery.

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.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Androgens play a key role in hair growth and disorders like baldness and excessive hairiness.

Taking vitamin B6 corrected a pregnant woman's metabolic disorder, which changed her hair color.

High levels of male hormones in pregnant mice cause heart enlargement and poor heart function in their female babies.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The document explains how hair is studied in forensics to identify its source and its role in criminal investigations.

Early over-expression of FoxN1 harms immune and skin development.

Diagnosing and treating PCOS in young people is difficult.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.