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Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

The document concludes that recognizing specific histological features of different nonscarring alopecias is crucial for accurate diagnosis and understanding hair loss progression.

Combination therapies for androgenetic alopecia work best but can have significant side effects and costs.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Early treatment of acne is crucial to prevent scarring and psychological effects.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

PCOS affects nearly 25% of female medical and dental students, impacting their academic and social lives.

Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

A man experienced hair loss from radiotherapy, which can be temporary or permanent depending on radiation dose, with potential treatments available.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

An infant with seizures and hair loss was diagnosed with biotinidase deficiency and treated successfully with biotin.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

Two siblings have a rare genetic condition causing curly, coarse hair.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A new gene mutation linked to a skin condition was found in a Spanish family.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

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

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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