Malformations.org

Synonyms:

• Hydrocephaly
• Hydrocephalia
• Congenital hydrocephalus

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

• Hypertelorism 4.35% (6/138 anomalies), in cases MDB47, MDB57, MDB100, MDB217, MDB322, MDB394
• Macrocephaly 4.35% (6/138 anomalies), in cases MDB47, MDB100, MDB202, MDB217, MDB60, MDB442
• Facial dysmorphism 3.62% (5/138 anomalies), in cases MDB47, MDB100, MDB202, MDB217, MDB394
• Low-set ears 2.9% (4/138 anomalies), in cases MDB47, MDB100, MDB217, MDB60
• Broad nasal bridge 2.9% (4/138 anomalies), in cases MDB47, MDB100, MDB502, MDB322
• Placenta hypoplasia 2.17% (3/138 anomalies), in cases MDB47, MDB100, MDB322
• Pulmonary hypoplasia 2.17% (3/138 anomalies), in cases MDB100, MDB202, MDB322
• Polydactyly of the hand, preaxial 2.17% (3/138 anomalies), in cases MDB60, MDB322, MDB322
• Overlapping fingers 1.45% (2/138 anomalies), in cases MDB100, MDB322
• Retrognathia 1.45% (2/138 anomalies), in cases MDB100, MDB394
• Microtia 1.45% (2/138 anomalies), in cases MDB202, MDB60
• Prominent and pointed nose 1.45% (2/138 anomalies), in cases MDB202, MDB217
• Cerebral ventriculomegaly 1.45% (2/138 anomalies), in cases MDB217, MDB60
• Micrognathia 1.45% (2/138 anomalies), in cases MDB217, MDB60
• Microcephaly 1.45% (2/138 anomalies), in cases MDB60, MDB322
• Cerebellar hypoplasia 1.45% (2/138 anomalies), in cases MDB60, MDB442
• Corpus callosum agenesis 1.45% (2/138 anomalies), in cases MDB502, MDB394
• Stenosis of aqueduct of Sylvius 0.72% (1/138 anomalies), in case MDB2
• Communicating hydrocephalus 0.72% (1/138 anomalies), in case MDB2
• Tetra-amelia 0.72% (1/138 anomalies), in case MDB47
• Lumbosacral agenesis 0.72% (1/138 anomalies), in case MDB47
• Thin upper lip 0.72% (1/138 anomalies), in case MDB47
• Exophthalmos, bilateral 0.72% (1/138 anomalies), in case MDB47
• Spina bifida occulta, lombosacral 0.72% (1/138 anomalies), in case MDB57
• Brainstem protuberance fibrosis 0.72% (1/138 anomalies), in case MDB57
• Flattened nose 0.72% (1/138 anomalies), in case MDB100
• Diaphragmatic hernia, congenital 0.72% (1/138 anomalies), in case MDB100
• Omphalocele 0.72% (1/138 anomalies), in case MDB100
• Intestinal malrotation 0.72% (1/138 anomalies), in case MDB100
• Renal focal cystic dilatation of collecting tubules 0.72% (1/138 anomalies), in case MDB100
• Placental hypermaturity 0.72% (1/138 anomalies), in case MDB156
• Unilobate lung, unilateral 0.72% (1/138 anomalies), in case MDB202
• Frontal bossing 0.72% (1/138 anomalies), in case MDB202
• Congenitally Corrected Transposition of the Great Arteries 0.72% (1/138 anomalies), in case MDB202
• Interauricular communication 0.72% (1/138 anomalies), in case MDB202
• Dandy-Walker malformation 0.72% (1/138 anomalies), in case MDB202
• Clindodactyly of 5th finger, bilateral 0.72% (1/138 anomalies), in case MDB217
• Epicanthus 0.72% (1/138 anomalies), in case MDB217
• Prominence of nasofrontal angle 0.72% (1/138 anomalies), in case MDB217
• Semilobar holoprosencephaly 0.72% (1/138 anomalies), in case MDB60
• Large anterior fontanelle 0.72% (1/138 anomalies), in case MDB60
• Badly-hemmed ears 0.72% (1/138 anomalies), in case MDB60
• Cleft palate with cleft lip (CLP), median 0.72% (1/138 anomalies), in case MDB60
• Hypogenesis of the Cerebellar Vermis 0.72% (1/138 anomalies), in case MDB60
• Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.72% (1/138 anomalies), in case MDB60
• Preauricular hamartoma 0.72% (1/138 anomalies), in case MDB60
• Cryptophthalmos 0.72% (1/138 anomalies), in case MDB60
• Flexion contracture of upper limbs 0.72% (1/138 anomalies), in case MDB60
• Dysplastic kidney with tubular cysts 0.72% (1/138 anomalies), in case MDB60
• absence of nasal septum 0.72% (1/138 anomalies), in case MDB60
• Hypoplasia of eye 0.72% (1/138 anomalies), in case MDB60
• skin hamartoma 0.72% (1/138 anomalies), in case MDB60
• Aqueduct of Sylvius atresia 0.72% (1/138 anomalies), in case MDB60
• Cerebral commissures agenesis 0.72% (1/138 anomalies), in case MDB60
• Stenosis of aortic valve 0.72% (1/138 anomalies), in case MDB502
• Cardiomegaly, fetal 0.72% (1/138 anomalies), in case MDB502
• Endocardial fibroelastosis 0.72% (1/138 anomalies), in case MDB502
• Hypoplasia of ascending aorta 0.72% (1/138 anomalies), in case MDB502
• Transverse aortic hypoplasia 0.72% (1/138 anomalies), in case MDB502
• Pleural effusion, fetal 0.72% (1/138 anomalies), in case MDB502
• Bicuspid aortic valve 0.72% (1/138 anomalies), in case MDB502
• Left ventricular hypertrophy, 0.72% (1/138 anomalies), in case MDB502
• Probst bundle 0.72% (1/138 anomalies), in case MDB502
• Defective developement of left ventricle 0.72% (1/138 anomalies), in case MDB147
• Mitral valve atresia 0.72% (1/138 anomalies), in case MDB147
• Aortic atresia 0.72% (1/138 anomalies), in case MDB147
• Patent Foramen Ovale 0.72% (1/138 anomalies), in case MDB147
• Persistent Ductus arteriosus 0.72% (1/138 anomalies), in case MDB147
• Clindodactyly of 5th finger, unilateral 0.72% (1/138 anomalies), in case MDB147
• Fissure of the upper gingiva, fetal 0.72% (1/138 anomalies), in case MDB147
• Periventricular Leukomalacia (PVL) 0.72% (1/138 anomalies), in case MDB147
• Intrauterine growth retardation, symmetric 0.72% (1/138 anomalies), in case MDB322
• Sloping forehead 0.72% (1/138 anomalies), in case MDB322
• Long philtrum 0.72% (1/138 anomalies), in case MDB322
• Gothic palate 0.72% (1/138 anomalies), in case MDB322
• Microretrognathia 0.72% (1/138 anomalies), in case MDB322
• Short neck 0.72% (1/138 anomalies), in case MDB322
• Neck edema 0.72% (1/138 anomalies), in case MDB322
• Camptodactyly, bilateral 0.72% (1/138 anomalies), in case MDB322
• Talipes equinovarus, bilateral 0.72% (1/138 anomalies), in case MDB322
• Syndactyly of the feet , simple (webbed), unilateral 0.72% (1/138 anomalies), in case MDB322
• Lower limb hyperextension, Fetal 0.72% (1/138 anomalies), in case MDB322
• Polysplenia 0.72% (1/138 anomalies), in case MDB322
• Gracile ribs 0.72% (1/138 anomalies), in case MDB322
• Wide space between 1st and 2nd toes, unilateral 0.72% (1/138 anomalies), in case MDB322
• Single umblical artery (SUA)-Isolated 0.72% (1/138 anomalies), in case MDB322
• Scoliosis, dextroconvex, thoracic 0.72% (1/138 anomalies), in case MDB322
• Neuronal migration anomaly 0.72% (1/138 anomalies), in case MDB322
• Cortical dysgenesis (CD), diffuse 0.72% (1/138 anomalies), in case MDB322
• Absence of neuron differentiation in the basal nuclei. 0.72% (1/138 anomalies), in case MDB322
• Flexion contracture of the fingers 0.72% (1/138 anomalies), in case MDB322
• Small round skull 0.72% (1/138 anomalies), in case MDB322
• Renal pelvis dilatation, bilateral 0.72% (1/138 anomalies), in case MDB394
• Bladder dilatation, fetal 0.72% (1/138 anomalies), in case MDB394
• Ureter hypoplasia 0.72% (1/138 anomalies), in case MDB394
• Stenosis of the mid ureter, congenital, left side 0.72% (1/138 anomalies), in case MDB394
• Hypospadias, penile 0.72% (1/138 anomalies), in case MDB394
• Hand edema 0.72% (1/138 anomalies), in case MDB394
• Foot edema 0.72% (1/138 anomalies), in case MDB394
• Intrauterine growth retardation, asymmetric 0.72% (1/138 anomalies), in case MDB442
• Pulmonary lobation anomalies 0.72% (1/138 anomalies), in case MDB442
• Monochorionic diamniotic placenta 0.72% (1/138 anomalies), in case MDB442
• Absence of the Septum Pellucidum 0.72% (1/138 anomalies), in case MDB442