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Insufficient androgen action in male fetuses can cause genital development issues due to genetic mutations or environmental chemicals.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

The document concludes that oral finasteride and topical minoxidil are effective for genetic hair loss, while other treatments for different types of hair loss show promise but need more research.

New treatments for hair loss are showing promise due to better understanding of genetics and the immune system.

FPHL is common in women, influenced by genetics and hormones, and can be treated with medications, laser therapy, or hair transplantation.

Polycystic Ovary Syndrome (PCOS) in teenagers is a complex condition linked to genetics and environment, often associated with obesity and insulin resistance, and is treated with lifestyle changes and medication.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Low-dose radiation affects hair stem cell function and survival by changing their genetic material's structure.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

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

Male pattern hair loss affects up to 80% of men due to genetics and hormone sensitivity.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

COVID-19 can lead to different skin symptoms and might trigger autoimmune diseases in genetically susceptible people.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Systemic immunotherapies are used for immune-related hair loss but not usually for genetic hair loss, unless the patient has both conditions.