Search

everythinglearnresearchcommunity

for

Search:↓

Early diagnosis and prednisone treatment can improve outcomes in Cronkhite-Canada syndrome.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

A man with follicular psoriasis got better after treatment with skin cream and allergy pills.

Advanced dermoscopy techniques improve diagnosis and treatment monitoring for Kerion celsi but don't guarantee full hair regrowth.

A mutation in the KRTHB5 gene causes hair and nail issues.

A rare case of scleredema in a diabetic woman showed loss of sweat glands, causing heat strokes, with treatment only slightly improving symptoms.

Biopsy is crucial for accurately diagnosing EPDS to avoid mistaking it for SCC.

The patient quickly recovered from hair loss caused by DRESS syndrome using topical minoxidil.

Frontal Fibrosing Alopecia may be linked to autoimmune diseases like Sjögren's syndrome.

Low vitamin C caused bleeding and corkscrew hair, resolved with vitamin C treatment.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

The document concludes that anticonvulsants like phenytoin may cause skin reactions by affecting tryptophan metabolism and suggests researching vitamin levels in patients with drug reactions.

Severe anti-TNF-α induced scalp eruptions often need stopping the drug and using systemic therapy to avoid scarring.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

Areata-like lupus can mimic alopecia areata but is a form of cutaneous lupus erythematosus.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

A boy developed a rare skin condition after recovering from a severe skin reaction, and it improved with lotion treatment.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Zinc deficiency causes skin issues and hair loss, treatable with zinc supplements.

Zinc deficiency was the real cause of the boy's symptoms, not a skin infection.

Patients with alopecia areata and eosinophilia have more nail issues and severe hair loss.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.