| congenital nonspherocytic hemolytic a. |
any of a heterogeneous group of inherited anemias characterized by shortened red blood cell survival, lack of spherocytosis, and normal osmotic fragility associated with erythrocyte membrane defects, multiple intracellular enzyme deficiencies or other defects, or unstable hemoglobins. The most common enzyme defects are in glucose-6-phosphate dehydrogenase or pyruvate kinase.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital p. |
Fanconi syndrome (def. 1).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital palatopharyngeal i. |
a congenital variety of velopharyngeal insufficiency.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital pernicious a. |
a rare disorder seen in children, clinically similar to the pernicious anemia of adults but differing in that gastric acid secretion is normal, the gastric mucosa is not atrophied, and development is delayed.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital photosensitive p. |
congenital erythropoietic p.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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