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Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Using old drugs for new uses can help treat rare immune deficiencies.

The document tests knowledge and decision-making in hematology through multiple-choice questions.

The document provides 70 multiple choice questions to improve haematology skills.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

Skin symptoms can indicate endocrine disorders and have various treatments.

The document concluded that stem cells are crucial for skin repair, regeneration, and may help in developing advanced skin substitutes.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

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

The mutation helps mice handle heat better without affecting hair growth.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Using animal names for skin conditions helps with learning and memory.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Vitamin D receptor helps control hair growth and could be used to treat certain skin tumors.

Vitamin D receptor may help protect against UV-induced skin cancer.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

Significant progress was made in understanding PXE, but effective treatments are still needed.