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Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

The endocannabinoid system affects oil production and inflammation in skin cells.

Eicosanoids are crucial for skin health, and targeting their pathways may help treat skin conditions.

Dermatologists play a key role in identifying and documenting signs of abuse and injury for forensic investigations.

Neurohormones help control skin health and could treat skin disorders.

The rash on the infant indicated a serious underlying condition.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

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.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

People with reproductive, thyroid disorders, and type 2 diabetes can experience voice changes, but more research is needed to understand this better.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Transplant success has improved with better immunosuppressive drugs and donor matching.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.