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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.

Skin color may change how alopecia areata looks under a dermoscope.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A blue Staffordshire Bull Terrier had hair loss due to color dilution alopecia, confirmed by tests, but no treatment was pursued.

A cat in Turkey had Ehlers-Danlos syndrome, showing very stretchy skin and easy bruising.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Trichoscopy is crucial for diagnosing and assessing alopecia areata in children.

A new gene mutation causes a rare type of hair loss.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A 6-year-old boy in India was diagnosed with Bloom's syndrome, showing growth and developmental issues, and skin problems worsened by sunlight.

Early investigation and a team approach are crucial for managing primary amenorrhea effectively.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

Androgens increase pigmentation in certain hamster skin areas, but estrogens can reverse this effect.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Ectopic acanthosis nigricans can occur at surgical sites due to skin graft mismatches.

Steroids, infection management, and nutritional support can significantly improve symptoms of Cronkhite-Canada Syndrome.

The girl had a rare disorder causing mental and physical symptoms, with weak hair and unclear neurological issues.

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

Tiger cubs fed artificial milk lacking certain amino acids developed eye problems and hair loss.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Thunbergia grandiflora and Russelia equisetiformis help each other grow by changing their shapes.

The document concludes that different patterns of hair thickness and scalp changes can help diagnose types of non-scarring hair loss.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Trichoscopy helps diagnose and assess the severity of two types of hair loss diseases, androgenetic alopecia and alopecia areata.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

Lowering homocyst(e)ine levels can reverse skin and hair lightening by restoring enzyme activity needed for pigmentation.