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Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Mutations in the AR gene cause hair thinning and loss.

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

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Genetic mutations can affect female sexual development, requiring personalized medical care.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Women with PCOS often have skin problems like excessive hair, acne, hair loss, and dark patches, which can be treated with hormonal and non-hormonal therapies.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Bone marrow-derived stem cells improved healing and reduced scarring in second-degree burns in rats.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

The document concludes that effectively managing PCOS requires a multifaceted approach.

Oxidative stress is a key factor in the development of Polycystic Ovary Syndrome, and weight management can improve symptoms.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Blocking a specific enzyme can reduce the negative impact of stress hormones on hair growth cells.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.