From: Birth defects in newborns and stillborns: an example of the Brazilian reality
Diagnosis | Number of cases | Etiology | |
---|---|---|---|
Newborns | Stillborns | ||
Multiple Defects | 10 | 5 | U |
Congenital Heart Disease | 9 | G/E | |
Down Syndrome | 9 | G | |
Gastroschisis | 8 | G/E | |
Neural Tube Defects | 7 | G/E | |
Foot-clubfoot | 5 | G/E | |
Amniotic Band Sequence | 4 | U | |
Disruption by Diabetes | 3 | E | |
Edwards Syndrome | 2 | 1 | G |
Orofacial Ccenter | 3 | G/E | |
Association VATERR | 2 | U | |
Esophageal Atresia | 2 | G/E | |
Fetal Alcohol Syndrome | 2 | E | |
Lung Cystic Adenomatous Malformation | 2 | U | |
Polydactyly (OMIM 603596) | 2 | G | |
Velocardiofacial Syndrome (OMIM 192430)* | 2 | G | |
Anorectal anomaly | 1 | G/E | |
Atelosteogenesis Type III (OMIM 108721)* | 1 | G | |
Biliary Atresia Extrahepatic (OMIM 210500) | 1 | U | |
Campomelic Dysplasia (OMIM 114290) | 1 | G | |
Camptodactyly (OMIM 114200) | 1 | G | |
Caudal Dysplasia Sequence | 1 | E | |
Colpocephaly | 1 | G/E | |
Congenital Aplasia Cutis (OMIM 107600) | 1 | G | |
Dandy-Walker (OMIM 22020) | 1 | G | |
Defects by Autosomal Recessive Inheritance* | 1 | G | |
DiGeorge syndrome (OMIM 188400) | 1 | G | |
Distal Arthrogryposis (OMIM 601680) | 1 | G | |
Duodenal atresia | 1 | U | |
Hypochondroplasia (OMIM 146000) | 1 | G | |
Imperforate Anus | 1 | G/E | |
Larsen Syndrome (OMIN 150250) | 1 | G | |
Laterality Sequence | 1 | U | |
Limb Body Wall Complex | 1 | U | |
Meckel Diverticulum | 1 | G/E | |
Möebius Sequence | 1 | U | |
Oculo-Auriculo-Vertebral Spectrum | 1 | U | |
Omphalocele | 1 | G/E | |
Patau Syndrome | 1 | G | |
Penoscrotal Hypospadia | 1 | G/E | |
Pfeiffer syndrome (OMIM 101600)* | 1 | G | |
Polythelia (OMIM 163700) | 1 | G | |
Prune Belly Syndrome (OMIM 100100) | 1 | G | |
Syndrome Barber-Say (OMIM 209885)* | 1 | G | |
Thanatophoric Dysplasia Type II (OMIM 187601) | 1 | G | |
Thoracic Dystrophy 1 (Jeune) (OMIM 208500) | 1 | G | |
Townes Brocks Syndrome (OMIM 107480) | 1 | G | |
X-Linked Hydrocephalus (OMIM 307000) | 1 | G |