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Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

The symptoms described align more with Haberland syndrome, not Delleman-Oorthuys syndrome.

Too much androgen can cause hair loss; finasteride may help.

T-cells in alopecia areata scalp show abnormal regulation, leading to less inflammation.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Different PCOS subgroups have similar metabolic features, but those without menstrual problems have milder issues.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

The conclusion is that there's a need for a new conference to establish stricter guidelines for diagnosing Polycystic Ovary Syndrome (PCOS).

Rosacea is a skin condition with unclear causes, classified into four subtypes.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

The machine learning model accurately predicts Systemic Lupus Erythematosus in Omani patients.

Special gels help heal diabetic foot sores and reduce the risk of amputation or death.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

ALRV5XR effectively increases hair density in men with androgenetic alopecia without adverse effects.

AR polyglycine repeat doesn't cause baldness.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Some skin medications are safe during pregnancy and breastfeeding, but others can harm the baby and should be avoided.

ALRV5XR effectively promotes hair regrowth in both men and women through different mechanisms.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

The document discusses how to diagnose and treat conditions like acne, excessive hair growth, and female pattern hair loss related to hormone imbalances.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.