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An adult with Kawasaki disease experienced temporary heart failure but recovered without lasting heart damage.

In a Tuscan pediatric clinic, 7.19% of children had hair or scalp disorders, with nonscarring alopecia being the most common.

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

An infant with scalp fungus was cured after extended treatment with antifungal medication.

Certain liver diseases respond well to specific treatments and have varying risks for liver cancer.

Caffeine improves hair growth, thickness, and reduces shedding.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Certain treatments can speed up local hair growth in mice but don't change the overall hair growth pattern.

Biomaterials combined with stem cells show promise for improving tissue repair and medical treatments.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

The review suggests renaming two herbs to avoid confusion and recommends more research for safe use.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

A hair tightly wrapped around a toddler's toe caused severe crying and was treated by surgery.

Topical corticosteroid was not more effective than placebo for children's alopecia areata, and atopy did not change treatment results.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

The Edwardian medical campaign linked maternal drinking to infant mortality and national decline, influencing hygiene education and leading to a ban on children under 14 from pubs.

A 3-year-old girl developed scurvy symptoms that improved with vitamin C but relapsed when supplementation stopped.

The conclusion is that Pigmented Epithelioid Melanocytoma can start from hair follicle stem cells or from a mole on the skin.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Erosive pustular dermatosis of the scalp is a rare condition that causes scarring hair loss, mainly in older women, and requires ongoing treatment.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

Using a special laser and skin medication together successfully cleared a skin condition in a pregnant woman.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

An elderly man's non-healing scalp lesion was successfully treated with a strong topical steroid.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Reflexology massage helps hair regrowth in women after chemotherapy.