Sanfilippo syndrome, glucose-6-phosphate dehydrogenase deficiency and sickle cell/β+ thalassemia in a child: The burden of consanguinity

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Veröffentlicht in:American journal of medical genetics. Part A 2014-01, Vol.164A (1), p.267-269
1. Verfasser: Mohamed, Sarar
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container_title American journal of medical genetics. Part A
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doi_str_mv 10.1002/ajmg.a.36180
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subjects Anemia, Sickle Cell - complications
Anemia, Sickle Cell - diagnosis
Anemia, Sickle Cell - genetics
beta-Thalassemia - complications
beta-Thalassemia - diagnosis
beta-Thalassemia - genetics
Child, Preschool
Consanguinity
Glucosephosphate Dehydrogenase Deficiency - complications
Glucosephosphate Dehydrogenase Deficiency - diagnosis
Glucosephosphate Dehydrogenase Deficiency - genetics
Humans
Male
Mucopolysaccharidosis III - complications
Mucopolysaccharidosis III - diagnosis
Mucopolysaccharidosis III - genetics
Pedigree
title Sanfilippo syndrome, glucose-6-phosphate dehydrogenase deficiency and sickle cell/β+ thalassemia in a child: The burden of consanguinity
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