A rare genetic disorder with sun-sensitive telangiectatic erythema on the face that evolves into poikiloderma, along with short stature and cancer risk.
A rare progeroid syndrome with a photosensitive rash that develops into poikiloderma, along with neurologic impairment and a 'cachectic dwarfism' appearance.
A rare genetic syndrome with a classic triad of nail dystrophy, oral leukoplakia, and a distinctive, reticulated (net-like) poikiloderma on the neck and chest.
The plaque stage of this cutaneous T-cell lymphoma can develop poikilodermatous features (atrophy, telangiectasia, pigment change) within the lesions.
An archaic term for a presentation that is now considered a form of poikilodermatous mycosis fungoides or connective tissue disease.
A common condition of chronic sun damage on the sides of the neck, with a characteristic mottled pattern of redness, hyper- and hypopigmentation, sparing the shaded area under the chin.
A rare genetic disorder with a characteristic poikilodermatous photosensitive rash in infancy, skeletal abnormalities, and increased cancer risk.
A genetic DNA repair disorder that leads to severe sun sensitivity and the early development of freckle-like hyperpigmentation and guttate hypopigmentation, creating a poikilodermatous appearance.
