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Chronic scalp lesions with crusts and pus indicate Erosive Pustular Dermatosis, which is confirmed by biopsy and effectively treated with strong topical steroids.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Soft-tissue calcification is rare in systemic lupus erythematosus.

New treatments and understanding of skin lupus are emerging in 2024.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

A young woman with visual issues and other symptoms was diagnosed with lupus and antiphospholipid syndrome, and improved with treatment.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Early treatment of pediatric lupus-related eye issues is crucial to prevent vision loss.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

A rare scalp condition called Erosive pustular dermatosis is hard to diagnose and treat.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

Hair dysplasias involve various hair disorders causing fragility, breakage, and poor hair adhesion.

Autoimmune conditions can be linked to trichoepitheliomas, with treatment focusing on cosmetic concerns.

A 54-year-old man with painful skin blisters and fever was diagnosed with Sweet syndrome and successfully treated with corticosteroids.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Uncombable hair syndrome is linked to Zellweger syndrome.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

Lipedematous scalp may have a genetic link and could be associated with psychiatric conditions.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Late onset SLE has different symptoms and antibody profiles compared to young onset SLE.

Certain skin symptoms can help detect and manage systemic lupus.