Malformations.org - View a developmental anomaly

Hypogenesis of the Cerebellar Vermis

DA: 337

Developmental anomaly information

Definition: Hypogenesis of the cerebellar vermis usually associated with Dandy-Walker malformation or Joubert syndrome.

Developmental anomaly parent: (empty)	Topology: Human body > Head and neck > Head > Cranium > Cerebellum
System: Human body > Nervous system > Central nervous system > Cerebellum	Developmental anomaly category: Anomaly of underdevelopment or overdevelopment

Case records MDB14, MDB69, MDB278, MDB309, MDB310, MDB60, MDB352, MDB359, MDB427, MDB443, MDB445, MDB514, MDB516, MDB542, MDB329, MDB288, MDB313, MDB290, MDB490, MDB509

Links

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 :

Low-set ears 3.76% (8/213 anomalies), in cases MDB69, MDB310, MDB60, MDB352, MDB359, MDB427, MDB443, MDB329
Cerebellar hypoplasia 3.29% (7/213 anomalies), in cases MDB309, MDB310, MDB60, MDB329, MDB288, MDB290, MDB490
Corpus callosum agenesis 2.82% (6/213 anomalies), in cases MDB14, MDB443, MDB445, MDB514, MDB516, MDB329
Pulmonary hypoplasia 2.82% (6/213 anomalies), in cases MDB69, MDB359, MDB443, MDB516, MDB329, MDB509
Facial dysmorphism 2.82% (6/213 anomalies), in cases MDB278, MDB352, MDB359, MDB427, MDB443, MDB329
Cerebral ventriculomegaly 2.35% (5/213 anomalies), in cases MDB69, MDB60, MDB445, MDB313, MDB490
Hypertelorism 2.35% (5/213 anomalies), in cases MDB69, MDB352, MDB514, MDB313, MDB490
Microcephaly 1.88% (4/213 anomalies), in cases MDB14, MDB60, MDB329, MDB509
Neck edema 1.88% (4/213 anomalies), in cases MDB69, MDB310, MDB443, MDB514
Intrauterine growth retardation, symmetric 1.88% (4/213 anomalies), in cases MDB278, MDB310, MDB359, MDB329
Placenta hypoplasia 1.88% (4/213 anomalies), in cases MDB278, MDB310, MDB359, MDB329
Tonsillar herniation of the cerebellum 1.88% (4/213 anomalies), in cases MDB352, MDB445, MDB288, MDB313
Polymicrogyria, focal 1.41% (3/213 anomalies), in cases MDB14, MDB329, MDB329
Dandy-Walker malformation 1.41% (3/213 anomalies), in cases MDB69, MDB352, MDB427
Clindodactyly of 5th finger, bilateral 1.41% (3/213 anomalies), in cases MDB69, MDB514, MDB490
Single umblical artery (SUA)-Isolated 1.41% (3/213 anomalies), in cases MDB278, MDB359, MDB427
Talipes equinovarus, bilateral 1.41% (3/213 anomalies), in cases MDB310, MDB445, MDB288
Absence of the Septum Pellucidum 1.41% (3/213 anomalies), in cases MDB443, MDB445, MDB516
Arnold-Chiari Type II malformation (CM II) 1.41% (3/213 anomalies), in cases MDB445, MDB542, MDB288
Myelomeningocele,lumbosacral with hydrocephalus 1.41% (3/213 anomalies), in cases MDB445, MDB542, MDB288
Thalamic nuclei centrum medianum fusion 0.94% (2/213 anomalies), in cases MDB14, MDB329
Macrocephaly 0.94% (2/213 anomalies), in cases MDB69, MDB60
Low nasal bridge 0.94% (2/213 anomalies), in cases MDB69, MDB443
Bladder hypoplasia 0.94% (2/213 anomalies), in cases MDB278, MDB310
Spina bifida occulta, lombosacral 0.94% (2/213 anomalies), in cases MDB278, MDB313
Camptodactyly, unilateral 0.94% (2/213 anomalies), in cases MDB278, MDB313
Long umbilical cord 0.94% (2/213 anomalies), in cases MDB278, MDB310
Hepatomegaly, fetal 0.94% (2/213 anomalies), in cases MDB309, MDB516
Micrognathia 0.94% (2/213 anomalies), in cases MDB310, MDB60
Lobulated, fused and horseshoe kidney 0.94% (2/213 anomalies), in cases MDB310, MDB359
Aqueduct of Sylvius atresia 0.94% (2/213 anomalies), in cases MDB60, MDB542
Communicating hydrocephalus 0.94% (2/213 anomalies), in cases MDB443, MDB313
Macroglossia 0.94% (2/213 anomalies), in cases MDB514, MDB313
Short neck 0.94% (2/213 anomalies), in cases MDB514, MDB329
Narrow thorax 0.94% (2/213 anomalies), in cases MDB514, MDB509
Holoprosencephaly, alobar 0.47% (1/213 anomalies), in case MDB14
Absence of the pyramid tracts, bilateral 0.47% (1/213 anomalies), in case MDB14
Hypotelorisme 0.47% (1/213 anomalies), in case MDB14
Obstetrician's hand 0.47% (1/213 anomalies), in case MDB14
Cleft palate with cleft lip,bilateral, complete 0.47% (1/213 anomalies), in case MDB14
Cleft lip, unilateral 0.47% (1/213 anomalies), in case MDB69
Syndactyly, simple (webbed), fingers 0.47% (1/213 anomalies), in case MDB69
Fingers amputation 0.47% (1/213 anomalies), in case MDB69
Holoprosencephaly 0.47% (1/213 anomalies), in case MDB69
Nasal hypoplasia 0.47% (1/213 anomalies), in case MDB69
Sloping forehead 0.47% (1/213 anomalies), in case MDB69
Constriction Ring Deformity of the upper limbs 0.47% (1/213 anomalies), in case MDB69
Syndactyly of the toes, complex, bilateral 0.47% (1/213 anomalies), in case MDB69
Constriction Ring Deformity of the lower limbs 0.47% (1/213 anomalies), in case MDB69
Ring constriction deformity of the toes 0.47% (1/213 anomalies), in case MDB69
Toes amputation 0.47% (1/213 anomalies), in case MDB69
Pterygium colli 0.47% (1/213 anomalies), in case MDB69
Nasal asymetria 0.47% (1/213 anomalies), in case MDB69
Gracile ribs 0.47% (1/213 anomalies), in case MDB69
Bowing of femur, congenital 0.47% (1/213 anomalies), in case MDB69
Nephromegaly, bilateral 0.47% (1/213 anomalies), in case MDB278
Multicystic renal dysplasia,bilateral 0.47% (1/213 anomalies), in case MDB278
Limbs hypoplasia 0.47% (1/213 anomalies), in case MDB278
Syndactyly of the toes, unilateral 0.47% (1/213 anomalies), in case MDB278
Toe hypoplasia, first, bilateral 0.47% (1/213 anomalies), in case MDB310
Ventricular septal defect, membranous 0.47% (1/213 anomalies), in case MDB310
Syndactyly of the feet , simple (webbed), unilateral 0.47% (1/213 anomalies), in case MDB310
Semilobar holoprosencephaly 0.47% (1/213 anomalies), in case MDB60
Large anterior fontanelle 0.47% (1/213 anomalies), in case MDB60
Badly-hemmed ears 0.47% (1/213 anomalies), in case MDB60
Microtia 0.47% (1/213 anomalies), in case MDB60
Cleft palate with cleft lip (CLP), median 0.47% (1/213 anomalies), in case MDB60
Hydrocephalus 0.47% (1/213 anomalies), in case MDB60
Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.47% (1/213 anomalies), in case MDB60
Preauricular hamartoma 0.47% (1/213 anomalies), in case MDB60
Cryptophthalmos 0.47% (1/213 anomalies), in case MDB60
Polydactyly of the hand, preaxial 0.47% (1/213 anomalies), in case MDB60
Flexion contracture of upper limbs 0.47% (1/213 anomalies), in case MDB60
Dysplastic kidney with tubular cysts 0.47% (1/213 anomalies), in case MDB60
absence of nasal septum 0.47% (1/213 anomalies), in case MDB60
Hypoplasia of eye 0.47% (1/213 anomalies), in case MDB60
skin hamartoma 0.47% (1/213 anomalies), in case MDB60
Cerebral commissures agenesis 0.47% (1/213 anomalies), in case MDB60
Stenosis of aqueduct of Sylvius 0.47% (1/213 anomalies), in case MDB352
Prominent and pointed nose 0.47% (1/213 anomalies), in case MDB352
Hydrocephalus, Non-communicating 0.47% (1/213 anomalies), in case MDB352
Retrognathia 0.47% (1/213 anomalies), in case MDB359
Triangular face 0.47% (1/213 anomalies), in case MDB359
Malformed ear 0.47% (1/213 anomalies), in case MDB359
Omphalocele 0.47% (1/213 anomalies), in case MDB359
Cystic dilatation of the fourth ventricle 0.47% (1/213 anomalies), in case MDB427
Broad nasal bridge 0.47% (1/213 anomalies), in case MDB427
Microretrognathia 0.47% (1/213 anomalies), in case MDB427
Aplasia cutis congenita, scalp 0.47% (1/213 anomalies), in case MDB427
Polydactyly of both fingers & toes, postaxial 0.47% (1/213 anomalies), in case MDB427
Coarctation of aorta, 0.47% (1/213 anomalies), in case MDB427
Anomalous pulmonary veins connection to superior & inferior vena cava 0.47% (1/213 anomalies), in case MDB427
Hypoplastic left atrium and ventricle 0.47% (1/213 anomalies), in case MDB427
Hypoplastic right atrium 0.47% (1/213 anomalies), in case MDB427
Bulbous nose 0.47% (1/213 anomalies), in case MDB443
Transverse palmar crease, bilateral 0.47% (1/213 anomalies), in case MDB443
Brachydactyly 0.47% (1/213 anomalies), in case MDB514
Hand edema 0.47% (1/213 anomalies), in case MDB514
Adrenal hypoplasia, fetal 0.47% (1/213 anomalies), in case MDB514
Splenic hypoplasia 0.47% (1/213 anomalies), in case MDB514
Foot edema 0.47% (1/213 anomalies), in case MDB514
Nonimmune hydrops fetalis (NIHF) 0.47% (1/213 anomalies), in case MDB516
Ascites, fetal 0.47% (1/213 anomalies), in case MDB516
Left-Sidedness, bilateral 0.47% (1/213 anomalies), in case MDB516
Intestinal malrotation 0.47% (1/213 anomalies), in case MDB516
Polysplenia 0.47% (1/213 anomalies), in case MDB516
Microsplenia 0.47% (1/213 anomalies), in case MDB516
Trilobate lung, left 0.47% (1/213 anomalies), in case MDB516
Placental hydrops 0.47% (1/213 anomalies), in case MDB516
Single cerebral ventricule 0.47% (1/213 anomalies), in case MDB516
Holoprosencephaly, lobar 0.47% (1/213 anomalies), in case MDB329
Megacystis 0.47% (1/213 anomalies), in case MDB329
Hydronephrosis, congenital, bilateral 0.47% (1/213 anomalies), in case MDB329
Dilatation of ureter , bilateral, congenital 0.47% (1/213 anomalies), in case MDB329
Flattened nose 0.47% (1/213 anomalies), in case MDB329
Long philtrum 0.47% (1/213 anomalies), in case MDB329
Prominent upper lip 0.47% (1/213 anomalies), in case MDB329
Cystic hygroma 0.47% (1/213 anomalies), in case MDB329
Arthrogryposis 0.47% (1/213 anomalies), in case MDB329
Hydromyelia 0.47% (1/213 anomalies), in case MDB329
Micromelia, lower limb, unilateral 0.47% (1/213 anomalies), in case MDB329
Ventricular septal defect, muscular 0.47% (1/213 anomalies), in case MDB329
Ureteral duplication, complete, unilateral 0.47% (1/213 anomalies), in case MDB313
Renal pelvis dilatation, unilateral 0.47% (1/213 anomalies), in case MDB313
Macrosomia 0.47% (1/213 anomalies), in case MDB290
Short rib polydactyly syndrome, type 1 0.47% (1/213 anomalies), in case MDB509
Short femur with angulated shaft 0.47% (1/213 anomalies), in case MDB509
Polydactyly,of the hand, postaxial 0.47% (1/213 anomalies), in case MDB509
Hypoplasia of optic nerve, bilateral 0.47% (1/213 anomalies), in case MDB509
Micromelia 0.47% (1/213 anomalies), in case MDB509
Olfactory bulbs hypoplasia 0.47% (1/213 anomalies), in case MDB509

Terminology and coding

References

No reference related to Hypogenesis of the Cerebellar Vermis is available at the moment.

Last modified: 2008-12-05 14:09:42 by farideh

Created: 2008-06-03 00:00:00 by phsaw

<< Previous anomaly entry

Next anomaly entry >>