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The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Human skin produces sex hormones like estrogen and testosterone, influenced by ARO and StAR, which may affect skin elasticity and hair growth.

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

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

New skin treatments in 1987-1988 showed effectiveness for various conditions, but some had side effects or risks.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

Steroid Sulfatase inhibitors show promise in treating hormone-dependent disorders like cancers, hair loss, and acne, with 667COUMATE being a potential candidate for breast cancer treatment trials.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

The document is a detailed medical reference on skin and genetic disorders.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Foam corticosteroid covers as well as traditional forms.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Pioglitazone improved insulin sensitivity and altered cortisol metabolism in PCOS patients.

Zinc pyrithione needs targeted delivery to the scalp for effective dandruff treatment.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Some skin diseases and their treatments can negatively affect male fertility.

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