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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The document suggests that the traditional understanding of hair growth cycles and alopecia may be inaccurate and that blood supply plays a significant role in hair growth and loss.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Humans lost body hair relatively recently in evolution.

Finasteride causes harmful organ changes in female mice.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

IL-2 treatment causes skin eruptions and other reversible side effects, and may play a role in psoriasis.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Pregnancy causes skin changes like darkening, hair thickening, nail changes, and increased risk of skin growths, most of which usually resolve after birth.

Msx2 and Foxn1 are both crucial for hair growth and health.

Finasteride increases hair weight and count in men with hair loss.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Dietary changes, including weight loss and a balanced diet, are important for managing PCOS, especially in overweight women.

Most pregnant women experience skin darkening and hair changes, with these effects usually going away after giving birth.

Early onset hair loss linked to genetics and androgen levels.

Small changes in hormones can significantly impact health, showing the importance of sensitive testing for chemicals that disrupt hormones.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Most pregnant women experience skin changes like darkening and itching, while serious skin conditions are rare but need early treatment.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Chemotherapy causes complex changes in hair follicle cells that can lead to hair loss.

Women with PCOS are at high risk of glucose metabolism issues and heart diseases, especially if overweight, highlighting the need for early intervention.