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The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Men with severe androgenetic alopecia, especially on the top of the head, have a higher risk of coronary artery disease.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

The document concludes that using a person's own fat cells (SVF) can significantly increase hair thickness and density, suggesting it could be a promising treatment for hair loss.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Videodermoscopy is effective for diagnosing different types of non-scarring hair loss.

Being overweight, having gallbladder removal surgery, and taking cholesterol-lowering drugs are linked to a higher chance of getting vulvar lichen sclerosus.

Alopecia can be reversed with timely steroid treatment in VKH and SO diseases.

When treating older patients with both heart valve disease and heart muscle disease, doctors should create personalized treatment plans that address both conditions.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A girl with Crohn's disease had a hairball causing bowel obstruction, which was removed, and she recovered well.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The conclusion is that cerebrovascular diseases can cause seizure-like activity in stroke patients, which can be improved with antiepileptic drugs.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

No single treatment is clearly effective for central serous chorioretinopathy.

Seborrheic dermatitis may contribute to the development of central centrifugal cicatricial alopecia.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Deucravacitinib helped regrow hair and reduce plaques in a woman with discoid lupus erythematosus without side effects.

Ivacaftor can protect against noise-induced hearing loss by reducing oxidative stress.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

Diabetic patients' stem cells make vascular grafts more prone to clots, but new methods may improve grafts.

Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

Understanding genetics is crucial for treating heart and skin diseases.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.