Cardiovascular: - Malformation
- Left heart hypoplasia
- Atrioventricular canal defect
- Right heart hypoplasia
- Closure of foramen ovale
- Single ventricle
- Transposition of the great arteries
- Ventricular septal defect
- Atrial septal defect
- Tetralogy of Fallot
- Ebstein's anomaly
- Premature closure of ductus
- Truncus arteriosus
- Aortic or pulmonary stenosis
- Valvular insufficiency
- AV canal defect
- Tachyarrhythmia
- Atrial flutter
- Paroxysmal atrial tachycardia
- Wolff-Parkinson-White
- Supraventricular tachycardia
- Bradyarrhythmia including complete heart block
- Other arrhythmia (eg, long QT)
- High-output failure
- Neuroblastoma
- Sacrococcygeal teratoma
- Large fetal angioma
- Placental chorioangioma
- Umbilical cord hemangioma
- Cardiac tumors
- Other cardiac neoplasia
- Cardiomyopathy
- Cardiosplenic syndromes
- Endocardial fibroelastosis
- 45, X
- Trisomy 21
- Trisomy 18
- Trisomy 13
- 18q +
- 13q –
- 45,X mosaic
- Triploidy
- 17q –
- Duplicated 11p
| Chondrodysplasias: - Thanatophoric dysplasia
- Short rib polydactyly
- Hypophosphatasia
- Osteogenesis imperfecta
- Achondrogenesis
- Camptomelic dysplasia
- Lethal chondroplasia
- Homozygous achondroplasia
- Twin-twin transfusion syndrome
- Acardiac twin
- Alpha-thalassemia
- Fetomaternal hemorrhage
- Parvovirus B19 infection
- Fetal hemorrhage
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency
- Glucose phosphate isomerase deficiency
- Red cell enzyme deficiencies
- Thrombosis of major vessels
- Leukemia
- Red cell aplasias
- Pyruvate kinase deficiency
- Spectrin protein abnormality or deficiency
- Transient myeloproliferative disorder
- Leukemoid reaction in response to congenital infection
- Kasabach-Merritt syndrome (microangiopathic hemolytic anemia, DIC)
- Blackfan Diamond anemia
- Lysosomal diseases
- Fanconi anemia
- Twin-twin transfusion syndrome, twin anemia-polycythemia sequence
- Congenital pulmonary airway malformation
- Diaphragmatic hernia
- Intrathoracic mass
- Pulmonary sequestration
- Chylothorax
- Airway obstruction
- Pulmonary lymphangiectasia
- Pulmonary neoplasia
- Bronchogenic cyst
- Cytomegalovirus
- Toxoplasmosis gondii
- Parvovirus B19
- Syphilis
- Herpes simplex virus
- Rubella virus
- Coxsackievirus
- Leptospirosis
- Trypanosoma cruzi
- Adenovirus
- Varicella
- Listeria
- Respiratory syncytial virus
- Congenital lymphocytic choriomeningitis virus
| Malformation sequences and genetic syndromes: - RASopathies (eg, Noonan's syndrome)
- Arthrogryposis
- Multiple pterygium syndrome
- Neu-Laxova syndrome
- Pena-Shokeir syndrome
- Myotonic dystrophy
- Saldino-Noonan syndrome
- Francois syndrome, type III
- Familial Nuchal Bleb
- Acrocephalopolydactylous dysplasia (Elejalde syndrome)
- Thoracoabdominal syndrome
- Lymphedema distichiasis syndrome
- CHARGE (coloboma, heart defect, atresia choanae, retardation of growth, ear abnormalities and deafness)
- Gaucher's disease
- GM1 gangliosidosis
- Sialidosis
- Hurler syndrome
- Mucopolysaccharide (MPS) IVa
- Mucolipidosis type I+II
- Galactosialidosis
- Urethral stenosis or atresia
- Posterior urethral valves
- Congenital nephrosis (Finnish type)
- Prune belly syndrome
- Midgut volvulus
- Malrotation of the intestines
- Duplication of the intestinal tract
- Meconium peritonitis
- Hepatic fibrosis
- Cholestasis
- Biliary atresia
- Jejunal atresia
- Hepatic vascular malformations
- Hepatitis
- Hepatic necrosis
- Liver tumors or cysts
- Intestinal tumor
- Gastrointestinal obstruction
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