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Intestinal malrotation

DA: 59

Developmental anomaly information

Definition: Congenital malformations of intestinal fixation(rotation): Many authors define intestinal malrotation as intestinal nonrotation or incomplete rotation around the superior mesenteric artery (SMA). It involves anomalies of intestinal fixation as well. Interruption of typical intestinal rotation and fixation during fetal development can occur at a wide range of locations, and this leads to a variety of both acute and chronic presentations of disease.

Synonyms:

intestinal malrotation, intestinal nonrotation, incomplete intestinal rotation, anomalies of intestinal fixation

Developmental anomaly parent: (empty)	Topology: Human body > Abdomen > Digestive tube > Small intestine
System: Human body > Digestive system > Small intestine	Developmental anomaly category: Malformation

Case records MDB5, MDB10, MDB100, MDB122, MDB125, MDB136, MDB379, MDB391, MDB402, MDB475, MDB477, MDB504, MDB516, MDB534, MDB301, MDB399

Links

Humpath: 7663

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

Associated genes in profile

Associated genes in malformative diseases

Associated chromosomal diseases

Associated signaling pathways

Associated developmental anomalies

Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :

Pulmonary hypoplasia 4.57% (9/197 anomalies), in cases MDB10, MDB100, MDB122, MDB125, MDB379, MDB391, MDB477, MDB516, MDB534
Facial dysmorphism 4.06% (8/197 anomalies), in cases MDB5, MDB100, MDB125, MDB136, MDB391, MDB402, MDB504, MDB399
Placenta hypoplasia 3.55% (7/197 anomalies), in cases MDB100, MDB122, MDB136, MDB379, MDB477, MDB504, MDB301
Retrognathia 3.05% (6/197 anomalies), in cases MDB100, MDB136, MDB391, MDB402, MDB504, MDB399
Low-set ears 2.54% (5/197 anomalies), in cases MDB100, MDB136, MDB402, MDB504, MDB399
Coarctation of aorta, 2.03% (4/197 anomalies), in cases MDB125, MDB136, MDB391, MDB402
Intrauterine growth retardation, symmetric 2.03% (4/197 anomalies), in cases MDB136, MDB391, MDB477, MDB399
Preauricular hamartoma 1.52% (3/197 anomalies), in cases MDB5, MDB391, MDB391
Macrocephaly 1.52% (3/197 anomalies), in cases MDB100, MDB125, MDB379
Hypertelorism 1.52% (3/197 anomalies), in cases MDB100, MDB125, MDB136
Defective developement of left ventricle 1.52% (3/197 anomalies), in cases MDB125, MDB136, MDB534
Nonimmune hydrops fetalis (NIHF) 1.52% (3/197 anomalies), in cases MDB125, MDB516, MDB534
Lobulated, fused and horseshoe kidney 1.52% (3/197 anomalies), in cases MDB391, MDB477, MDB399
Pulmonary artery hypoplasia 1.52% (3/197 anomalies), in cases MDB475, MDB477, MDB504
Epicanthus 1.02% (2/197 anomalies), in cases MDB5, MDB125
Transverse palmar crease, bilateral 1.02% (2/197 anomalies), in cases MDB5, MDB125
Ventricular septal defect, membranous 1.02% (2/197 anomalies), in cases MDB5, MDB10
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 1.02% (2/197 anomalies), in cases MDB5, MDB379
Dilatation of ureter , bilateral, congenital 1.02% (2/197 anomalies), in cases MDB5, MDB125
Microsplenia 1.02% (2/197 anomalies), in cases MDB5, MDB516
Cystic hygroma 1.02% (2/197 anomalies), in cases MDB5, MDB391
Talipes equinovarus, bilateral 1.02% (2/197 anomalies), in cases MDB5, MDB391
Amnion nodosum 1.02% (2/197 anomalies), in cases MDB5, MDB402
Polysplenia 1.02% (2/197 anomalies), in cases MDB5, MDB516
Persistent left superior vena cava 1.02% (2/197 anomalies), in cases MDB10, MDB122
Absence of innominate (brachiocephalic) vein 1.02% (2/197 anomalies), in cases MDB10, MDB122
Diaphragmatic hernia, congenital 1.02% (2/197 anomalies), in cases MDB100, MDB122
Overlapping fingers 1.02% (2/197 anomalies), in cases MDB100, MDB399
Broad nasal bridge 1.02% (2/197 anomalies), in cases MDB100, MDB504
Polydactyly of both fingers & toes, postaxial 1.02% (2/197 anomalies), in cases MDB136, MDB534
Dextrocardia, isolated 1.02% (2/197 anomalies), in cases MDB391, MDB475
Ventricular septal defect, muscular 1.02% (2/197 anomalies), in cases MDB391, MDB399
Cleft palate with cleft lip,bilateral, complete 1.02% (2/197 anomalies), in cases MDB402, MDB301
Syndactyly of the fingers, complex, bilateral 1.02% (2/197 anomalies), in cases MDB402, MDB477
Syndactyly of the toes, complex, bilateral 1.02% (2/197 anomalies), in cases MDB477, MDB534
Ascites, fetal 1.02% (2/197 anomalies), in cases MDB516, MDB534
Hypoplasia of ascending aorta 1.02% (2/197 anomalies), in cases MDB534, MDB301
Flat face 0.51% (1/197 anomalies), in case MDB5
Flattened occiput 0.51% (1/197 anomalies), in case MDB5
Macroglossia 0.51% (1/197 anomalies), in case MDB5
Atrial Hypertrophy 0.51% (1/197 anomalies), in case MDB5
Overlapping toes 0.51% (1/197 anomalies), in case MDB5
Fusion of the adrenal glands 0.51% (1/197 anomalies), in case MDB5
Lung agenesis, unilateral 0.51% (1/197 anomalies), in case MDB5
Unilobate lung, unilateral 0.51% (1/197 anomalies), in case MDB5
Bladder wall thickness 0.51% (1/197 anomalies), in case MDB5
Pentalogy of Cantrell 0.51% (1/197 anomalies), in case MDB10
Defects of the lower part of the sternum 0.51% (1/197 anomalies), in case MDB10
Hydrocephalus 0.51% (1/197 anomalies), in case MDB100
Flattened nose 0.51% (1/197 anomalies), in case MDB100
Omphalocele 0.51% (1/197 anomalies), in case MDB100
Renal focal cystic dilatation of collecting tubules 0.51% (1/197 anomalies), in case MDB100
Anencephaly 0.51% (1/197 anomalies), in case MDB122
Aberrant right subclavian artery 0.51% (1/197 anomalies), in case MDB122
Atrioventricular - channel 0.51% (1/197 anomalies), in case MDB125
Hypoplasia of the aortic isthmus 0.51% (1/197 anomalies), in case MDB125
Pulmonary artery dilatation, fetal 0.51% (1/197 anomalies), in case MDB136
Aortic valve stenosis, congenital 0.51% (1/197 anomalies), in case MDB136
Right ventricle dilatation 0.51% (1/197 anomalies), in case MDB136
Right atrium Enlargement 0.51% (1/197 anomalies), in case MDB136
Single transverse palmar crease, unilateral 0.51% (1/197 anomalies), in case MDB136
Clindodactyly of 5th finger, unilateral 0.51% (1/197 anomalies), in case MDB136
Meckel diverticulum 0.51% (1/197 anomalies), in case MDB136
Renal hypoplasia 0.51% (1/197 anomalies), in case MDB379
Renal ectopia, simple 0.51% (1/197 anomalies), in case MDB379
Placenta circumvallata 0.51% (1/197 anomalies), in case MDB379
Cardiac hypoplasia, fetal 0.51% (1/197 anomalies), in case MDB379
Absence of first fingers, bilateral 0.51% (1/197 anomalies), in case MDB379
Prominent and pointed nose 0.51% (1/197 anomalies), in case MDB391
Anotia 0.51% (1/197 anomalies), in case MDB391
Absence of diaphragm, left 0.51% (1/197 anomalies), in case MDB391
Clindodactyly of 5th finger, bilateral 0.51% (1/197 anomalies), in case MDB391
Pterygium colli 0.51% (1/197 anomalies), in case MDB391
Pectus excavatum 0.51% (1/197 anomalies), in case MDB391
Single umblical artery (SUA)-Isolated 0.51% (1/197 anomalies), in case MDB391
Fraser syndrome 0.51% (1/197 anomalies), in case MDB402
Toe hypoplasia, first, bilateral 0.51% (1/197 anomalies), in case MDB402
Subglottic Stenosis (CSS) 0.51% (1/197 anomalies), in case MDB402
Non-segmented lung 0.51% (1/197 anomalies), in case MDB402
Ureter agenesis, bilateral 0.51% (1/197 anomalies), in case MDB402
Renal agenesis, bilateral 0.51% (1/197 anomalies), in case MDB402
Bladder agenesis 0.51% (1/197 anomalies), in case MDB402
Left side appendix 0.51% (1/197 anomalies), in case MDB402
Micropenis 0.51% (1/197 anomalies), in case MDB402
Imperforate Anus 0.51% (1/197 anomalies), in case MDB402
Pyloric stenosis 0.51% (1/197 anomalies), in case MDB402
Bilateral Right-Sidedness Sequence 0.51% (1/197 anomalies), in case MDB475
Asplenia 0.51% (1/197 anomalies), in case MDB475
Quadrilobated lung, bilateral 0.51% (1/197 anomalies), in case MDB475
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.51% (1/197 anomalies), in case MDB477
Relative Macrocephaly 0.51% (1/197 anomalies), in case MDB477
Pulmonary lobation anomalies 0.51% (1/197 anomalies), in case MDB477
Ambiguous genitalia 0.51% (1/197 anomalies), in case MDB477
Clitoris hyperplasia 0.51% (1/197 anomalies), in case MDB477
Adrenal hypoplasia, fetal 0.51% (1/197 anomalies), in case MDB477
Cleft palate with cleft lip (CLP), median 0.51% (1/197 anomalies), in case MDB504
Cutaneous bud 0.51% (1/197 anomalies), in case MDB504
Hypotelorisme 0.51% (1/197 anomalies), in case MDB504
Aplasia cutis congenita, scalp 0.51% (1/197 anomalies), in case MDB504
Camptodactyly, bilateral 0.51% (1/197 anomalies), in case MDB504
Tetralogy of Fallot 0.51% (1/197 anomalies), in case MDB504
Pulmonary valve atresia 0.51% (1/197 anomalies), in case MDB504
Dextroposition of aorta 0.51% (1/197 anomalies), in case MDB504
Right ventricular hypertrophy 0.51% (1/197 anomalies), in case MDB504
Left-Sidedness, bilateral 0.51% (1/197 anomalies), in case MDB516
Trilobate lung, left 0.51% (1/197 anomalies), in case MDB516
Hepatomegaly, fetal 0.51% (1/197 anomalies), in case MDB516
Placental hydrops 0.51% (1/197 anomalies), in case MDB516
Hypogenesis of the Cerebellar Vermis 0.51% (1/197 anomalies), in case MDB516
Single cerebral ventricule 0.51% (1/197 anomalies), in case MDB516
Corpus callosum agenesis 0.51% (1/197 anomalies), in case MDB516
Absence of the Septum Pellucidum 0.51% (1/197 anomalies), in case MDB516
Short rib polydactyly syndrome, type 1 0.51% (1/197 anomalies), in case MDB534
Narrow thorax 0.51% (1/197 anomalies), in case MDB534
Micromelia 0.51% (1/197 anomalies), in case MDB534
Aortic valve atresia 0.51% (1/197 anomalies), in case MDB534
Mitral valve stenosis 0.51% (1/197 anomalies), in case MDB534
Large nose, fetal 0.51% (1/197 anomalies), in case MDB534
Low nasal bridge 0.51% (1/197 anomalies), in case MDB534
Short neck 0.51% (1/197 anomalies), in case MDB534
Polydactyly,of the hand, postaxial 0.51% (1/197 anomalies), in case MDB301
Aberrant left subclavian artery 0.51% (1/197 anomalies), in case MDB301
Bicornuate uterus 0.51% (1/197 anomalies), in case MDB301
Triangular face 0.51% (1/197 anomalies), in case MDB399

Terminology and coding

	WHO ICD-10: Q43.3

References

No reference related to Intestinal malrotation is available at the moment.

Last modified: 2008-12-12 16:12:49 by farideh

Created: 2008-02-25 00:00:00 by phsaw

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