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The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Horizontal sections of scalp biopsies are good for diagnosing Central Centrifugal Cicatricial Alopecia and help customize treatment.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Researchers found a new sign of fungal infection in some patients with Seborrheic Dermatitis.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Scalp sarcoidosis can cause hair loss and needs accurate diagnosis and treatment with specific medications.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Alopecia areata mainly affects young people and has significant psychological impacts, especially in males.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

Trichoscopy can help diagnose early congenital syphilis in newborns.

Seborrhoeic dermatitis may cause a condition called "seborrhoeic folliculitis," leading to chronic scalp inflammation and scarring hair loss.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

Including special area involvement helps identify more psoriasis patients who may need systemic treatment.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Erosive pustular dermatosis of the scalp may not be as rare as previously thought.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

The conclusion is that skin, mucous, and eye problems after Stevens-Johnson syndrome and Lyell syndrome significantly affect patients' lives, highlighting the need for comprehensive care and eye check-ups.

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

A woman with lupus experienced hair regrowth after treatment, but hair transplantation is not advised for her condition.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

No single treatment is clearly effective for central serous chorioretinopathy.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The conclusion is that Erosive Pustular Dermatosis of the Scalp is a rare condition best treated with strong topical steroids and sometimes systemic treatment.