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glucose-6-phosphate dehydrogenase (G6PD) deficiency, an X-linked disorder, is more common in families of Mediterranean or West African origin than in other ethnic groups.
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CLIPP 8 - neonatal jaundice
cell anemia) These disorders have varied modes of inheritance (X-linked, autosomal dominant, autosomal recessive) and may be found with greater prevalence among certain ethnicities, or in certain parts of the world. For example, <span>glucose-6-phosphate dehydrogenase (G6PD) deficiency, an X-linked disorder, is more common in families of Mediterranean or West African origin than in other ethnic groups. Biliary Atresia A healthy-appearing infant who develops jaundice, dark urine, and acholic (pale) stools between 3 and 6 weeks of age may have biliary atresia.


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