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Gastroenterology Clinics of North America, 2003
Neonatal hemochromatosis is a rare gestational condition in which iron accumulates in the fetal tissues in a distribution like that seen in hereditary hemochromatosis. Extensive liver damage is the dominant clinical feature, with late fetal loss or early neonatal death. NH recurs within sibships at a rate higher than that predicted for simple Mendelian
Knisely, A S +2 more
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Neonatal hemochromatosis is a rare gestational condition in which iron accumulates in the fetal tissues in a distribution like that seen in hereditary hemochromatosis. Extensive liver damage is the dominant clinical feature, with late fetal loss or early neonatal death. NH recurs within sibships at a rate higher than that predicted for simple Mendelian
Knisely, A S +2 more
openaire +3 more sources
Archives of Dermatology, 1964
The case history of a 47-year-old male patient with vitiligo and hemochromatosis is reported. Skin biopsies disclose the uniform distribution of iron pigmentation, although the vitiligo spots seem to be deficient in melanin as opposed to the dark-colored skin areas where contents of melanin apparently have increased.
A, PERDRUP, H, POULSEN
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The case history of a 47-year-old male patient with vitiligo and hemochromatosis is reported. Skin biopsies disclose the uniform distribution of iron pigmentation, although the vitiligo spots seem to be deficient in melanin as opposed to the dark-colored skin areas where contents of melanin apparently have increased.
A, PERDRUP, H, POULSEN
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Annals of Internal Medicine, 1957
Excerpt In Sheldon's1classic monograph on hemochromatosis, myocardial failure is mentioned as an uncommon cause of death.
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Excerpt In Sheldon's1classic monograph on hemochromatosis, myocardial failure is mentioned as an uncommon cause of death.
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Archives of Internal Medicine, 1986
Hemochromatosis is a hereditary disorder of the control of iron metabolism wherein the absorptive intestine accepts from the diet more iron than the body requires; because no excretory mechanism exists, the excess must be deposited in storage organs, ultimately to their detriment.
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Hemochromatosis is a hereditary disorder of the control of iron metabolism wherein the absorptive intestine accepts from the diet more iron than the body requires; because no excretory mechanism exists, the excess must be deposited in storage organs, ultimately to their detriment.
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Nursing Clinics of North America, 2000
Hereditary hemochromatosis (HH) is an autosomal recessive iron overload disorder that affects more than one million Americans. This underdiagnosed disorder is associated with high morbidity and mortality, which can be prevented with early identification and treatment.
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Hereditary hemochromatosis (HH) is an autosomal recessive iron overload disorder that affects more than one million Americans. This underdiagnosed disorder is associated with high morbidity and mortality, which can be prevented with early identification and treatment.
openaire +2 more sources

