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Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

Segmental Vitiligo is a stable, early-onset form of vitiligo that responds well to early treatment and is ideal for repigmentation studies.

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

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Hair growth dysfunction involves various conditions with limited treatment options.

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

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The document concludes that various hair disorders have different treatments, including medication, surgery, and addressing underlying causes.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Using platelet growth factors can improve hair density in transplants, especially for those with fine hair.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Nanoliposomes effectively deliver hair-growth peptides into hair follicles.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Combining PRP with lipofilling shows promise for tissue regeneration but needs more clinical trials to confirm benefits.

Controlling Tslp can improve health in AEC syndrome patients.