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Sulfasalazine can cause severe allergic reactions leading to long-term autoimmune issues like hair loss and skin discoloration.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

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

Lupus can cause unusual vision problems, so it's important to consider it in such cases.

A woman with Kallman's syndrome also developed alopecia universalis, a condition not previously linked to Kallman's.

The boy likely has a fungal infection causing hair loss.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

Metastatic cervical cancer can cause rare, severe Cushing's syndrome with high risk of death.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

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

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A woman developed lupus after taking hydroxyurea for two years.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

A rare tumor caused unusual hormone production leading to Cushing syndrome.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

Steroid pulse therapy improved symptoms in a man with Satoyoshi syndrome.

Norfolk Terriers have a genetic skin defect causing scaling and blisters due to a keratin issue.

A 5-year-old boy has Nevus Comedonicus Syndrome, causing skin lesions and a cataract.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Epidermal nevi are skin cell clusters linked to various syndromes.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

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

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A 22-year-old with multiple autoimmune diseases needs a multidisciplinary treatment approach.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Secukinumab treatment may cause HBV reactivation and hair discoloration.