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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

No link found between Coxsackie viruses and pemphigus.

Vesiculobullous lesions should be considered part of canine cutaneous epitheliotropic T-cell lymphoma.

Tofacitinib helped over half of the patients with severe hair loss regrow at least 50% of their hair.

Hair loss is a rare but recognized symptom of pemphigus vulgaris, with patients usually regrowing hair after treatment.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

VB1953 gel significantly reduced acne and resistant bacteria in patients who didn't respond to clindamycin.

Sandalore®, a synthetic scent, improved hair loss and satisfaction in women with telogen effluvium.

Correcting nutrient deficiencies may help with hair loss, but the benefits of supplements without a deficiency are uncertain and could be harmful.

An 18-year-old girl with pemphigus vulgaris needed strong medication and careful treatment due to ineffective initial therapies and side effects.

A 7-year-old dog with a rare autoimmune disease was euthanized due to severe anemia and poor prognosis.

The conclusion of the case is not provided in the summary.

Some cancer and immune system drugs can cause serious side effects, including heart, lung, nerve, and organ damage, which need careful monitoring and management.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

Some drugs can cause skin, nail, and hair problems, which are important for healthcare professionals to recognize and report.

Botulinum toxin has potential for treating various skin conditions and improving wound healing.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

MG53 helps reduce skin damage caused by nitrogen mustard.

Biologic treatments for Crohn's disease and ulcerative colitis can cause skin problems, and doctors should adjust treatment if these occur.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

The first book is useful for specialized dermatologists but not for common issues, while the second book is good for medical students despite some errors.

Effective treatment for hidradenitis suppurativa varies, with antibiotics commonly used and surgery as an option, but no single method is universally successful.

Two patients with porphyria cutanea tarda experienced their grey hair turning dark again.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.