Journal of Clinical Pathology · 1994 · 28 citations · 9 references
MedicineDermatologyPathologyDermatopathologyHuman GeneticsMicronutrient DeficiencyCongenital Skin DisordersPigmentary DisordersVitamin B12 DeficiencyCongenital Pigmentary DisordersGenetic Disorders Of Vitamin MetabolismPigment-related DermatosesPoikiloderma SyndromesSkin Pigmentation DisordersVitamin Deficiency Syndromes
Two brothers in a Chinese family with selective malabsorption of vitamin B12 associated with proteinuria (Imerslund-Grasbeck syndrome) presented with widespread mottled skin pigmentation, termed poikiloderma. In contrast to anaemia, this pigmentary disturbance remained unresponsive to vitamin B12 replacement. This is different from the reported hyperpigmentation sometimes seen in vitamin B12 deficiency which is reversible following treatment. As far as is known, an irreversible and persistent skin disorder has not been reported in this syndrome before.
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Selective Vitamin B<sub>12</sub> Malabsorption and Proteinuria in Young People A Syndrome
Ralph Gräsbeck, Ruben Gordin, I. KANTERO et al. · Acta Medica Scandinavica · 1960 · 231 citations
Medicine, Nephrology, Pediatrics +12
Idiopathic Chronic Megaloblastic Anemia in Children
Olga Imerslund · Acta Paediatrica · 1960 · 176 citations
Medicine, Hematology, Pediatrics +11
Simon Baker, M. Ignatius, S F Johnson et al. · BMJ · 1963 · 78 citations
Medicine, Neurology, Pharmacotherapy +12
Harald Broch, Olga Imerslund, E. Monn et al. · Acta Paediatrica · 1984 · 78 citations
Medicine, Nephrology, Pediatrics +16