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MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Telogen Effluvium is a common hair loss condition, particularly in women, with no specific FDA-approved treatment, and recovery can take up to 18 months.

Biotin supplements are unnecessary for most people but may help with certain conditions like biotin deficiency, brittle nails, and some hair loss.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Genetics can help tailor treatments for male pattern hair loss, improving outcomes like stabilization or modest regrowth.

Hair shaft disorders often indicate genetic or systemic issues and are managed by minimizing damage.

Understanding embryologic layers improves skin disorder diagnosis and supports developing targeted therapies.

A young athlete's fragile hair condition improved by cutting hair and using gentle shampoo.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Hormone treatment caused hair loss, finasteride helped regrowth.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

A new system helps better diagnose and treat female androgenization conditions like PCOS.

Bone Morphogenetic Proteins (BMPs) help control skin health, hair growth, and color, and could potentially be used to treat skin and hair disorders.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Researchers identified specific genes that are important for mouse skin cell development and healing.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

The document does not determine if adults with aphallia are fertile.

Trichoscopy is a useful tool for diagnosing different hair and scalp diseases by their unique visual features.

Alopecia areata is a type of hair loss that can lead to complete baldness, often associated with other autoimmune conditions, and half of the cases may see hair return within a year.

AGA can occur in children with family history; early diagnosis and treatment important.

Epidermal stem cells could lead to new treatments for skin and hair disorders.