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A new gene variant in the DSP gene is linked to a unique type of hair loss.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Alopecia Areata is a complex, unpredictable autoimmune hair loss condition with limited treatment options and a significant psychological impact.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Hair loss in cancer patients can be related to the cancer itself, treatment, or other conditions, and understanding it is important for diagnosis and patient care.

Finasteride may effectively treat hair loss in Klinefelter Syndrome patients.

Hair loss risk is influenced by multiple genes.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Nursing staff's mental health was affected during the COVID-19 pandemic.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

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

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.