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Retrognathia

DA: 67

Developmental anomaly information

Definition: Retrognathia: Retrusion of the mandible which is the one of the anomalies of jaw-cranial base relationship

Synonyms:

Retrognathism
receding chin

Developmental anomaly parent: (empty)	Topology: Human body > Head and neck > Head > Face > Mouth
System: Human body > musculoskeletal system.	Developmental anomaly category: Malformation

Case records MDB21, MDB40, MDB50, MDB114, MDB136, MDB339, MDB168, MDB178, MDB255, MDB265, MDB279, MDB330, MDB332, MDB350, MDB368, MDB358, MDB359, MDB360, MDB367, MDB391, MDB394, MDB397, MDB399, MDB400, MDB402, MDB430, MDB431, MDB436, MDB437, MDB438, MDB456, MDB466, MDB470, MDB471, MDB472, MDB476, MDB481, MDB487, MDB503, MDB504, MDB506, MDB518, MDB524, MDB543, MDB90, MDB146, MDB161, MDB262, MDB270, MDB100

Links

Humpath: 6525

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 :

Facial dysmorphism 6.79% (34/501 anomalies), in cases MDB21, MDB40, MDB50, MDB136, MDB339, MDB168, MDB178, MDB279, MDB332, MDB350, MDB358, MDB359, MDB360, MDB367, MDB391, MDB394, MDB397, MDB399, MDB402, MDB431, MDB437, MDB456, MDB466, MDB470, MDB471, MDB481, MDB487, MDB504, MDB506, MDB518, MDB524, MDB543, MDB270, MDB100
Low-set ears 4.19% (21/501 anomalies), in cases MDB21, MDB136, MDB339, MDB168, MDB332, MDB350, MDB359, MDB399, MDB402, MDB437, MDB470, MDB471, MDB476, MDB503, MDB504, MDB506, MDB518, MDB543, MDB146, MDB270, MDB100
Intrauterine growth retardation, symmetric 3.59% (18/501 anomalies), in cases MDB136, MDB339, MDB168, MDB265, MDB332, MDB368, MDB358, MDB359, MDB367, MDB391, MDB399, MDB431, MDB471, MDB472, MDB476, MDB481, MDB161, MDB270
Pulmonary hypoplasia 2.99% (15/501 anomalies), in cases MDB50, MDB114, MDB168, MDB359, MDB367, MDB391, MDB438, MDB456, MDB471, MDB472, MDB487, MDB503, MDB518, MDB524, MDB100
Placenta hypoplasia 2.4% (12/501 anomalies), in cases MDB40, MDB136, MDB339, MDB255, MDB332, MDB358, MDB359, MDB471, MDB503, MDB504, MDB543, MDB100
Hypertelorism 2.2% (11/501 anomalies), in cases MDB50, MDB136, MDB178, MDB368, MDB358, MDB367, MDB394, MDB481, MDB161, MDB270, MDB100
Prominent and pointed nose 2.2% (11/501 anomalies), in cases MDB332, MDB360, MDB391, MDB430, MDB431, MDB436, MDB437, MDB466, MDB470, MDB487, MDB524
Short neck 1.6% (8/501 anomalies), in cases MDB40, MDB368, MDB367, MDB470, MDB476, MDB487, MDB506, MDB270
Toe hypoplasia, first, bilateral 1.6% (8/501 anomalies), in cases MDB330, MDB350, MDB368, MDB402, MDB430, MDB438, MDB146, MDB161
Low nasal bridge 1.6% (8/501 anomalies), in cases MDB350, MDB368, MDB397, MDB438, MDB470, MDB471, MDB472, MDB146
Clindodactyly of 5th finger, bilateral 1.4% (7/501 anomalies), in cases MDB168, MDB279, MDB350, MDB368, MDB391, MDB481, MDB487
Lobulated, fused and horseshoe kidney 1.4% (7/501 anomalies), in cases MDB265, MDB332, MDB359, MDB391, MDB399, MDB487, MDB262
Neck edema 1.4% (7/501 anomalies), in cases MDB279, MDB368, MDB367, MDB470, MDB476, MDB506, MDB543
Coarctation of aorta, 1.2% (6/501 anomalies), in cases MDB136, MDB178, MDB367, MDB391, MDB402, MDB262
Intestinal malrotation 1.2% (6/501 anomalies), in cases MDB136, MDB391, MDB399, MDB402, MDB504, MDB100
Wide space between 1st and 2nd toes, bilateral 1.2% (6/501 anomalies), in cases MDB279, MDB367, MDB437, MDB456, MDB466, MDB470
Triangular face 1.2% (6/501 anomalies), in cases MDB332, MDB359, MDB399, MDB430, MDB431, MDB437
Large anterior fontanelle 1.2% (6/501 anomalies), in cases MDB431, MDB470, MDB471, MDB476, MDB487, MDB543
Potter's facies 1% (5/501 anomalies), in cases MDB255, MDB438, MDB472, MDB90, MDB146
Potter deformity sequence 1% (5/501 anomalies), in cases MDB255, MDB438, MDB472, MDB503, MDB90
Single umblical artery (SUA)-Isolated 1% (5/501 anomalies), in cases MDB358, MDB359, MDB391, MDB487, MDB262
Posteriorly inclined and low-positioned ears 0.8% (4/501 anomalies), in cases MDB40, MDB481, MDB487, MDB524
Broad nasal bridge 0.8% (4/501 anomalies), in cases MDB40, MDB50, MDB504, MDB100
Talipes equinovarus, bilateral 0.8% (4/501 anomalies), in cases MDB50, MDB114, MDB391, MDB431
Macrocephaly 0.8% (4/501 anomalies), in cases MDB50, MDB358, MDB437, MDB100
Clindodactyly of 5th finger, unilateral 0.8% (4/501 anomalies), in cases MDB136, MDB367, MDB518, MDB146
Adrenal hypoplasia, fetal 0.8% (4/501 anomalies), in cases MDB168, MDB358, MDB367, MDB487
Imperforate Anus 0.8% (4/501 anomalies), in cases MDB255, MDB402, MDB481, MDB262
Flattened nose 0.8% (4/501 anomalies), in cases MDB255, MDB456, MDB90, MDB100
Transverse palmar crease, bilateral 0.8% (4/501 anomalies), in cases MDB265, MDB368, MDB481, MDB146
Narrow thorax 0.8% (4/501 anomalies), in cases MDB358, MDB471, MDB487, MDB518
Ureteral duplication, complete, unilateral 0.8% (4/501 anomalies), in cases MDB358, MDB481, MDB487, MDB146
Overlapping fingers 0.8% (4/501 anomalies), in cases MDB399, MDB518, MDB161, MDB100
Dolicocephaly 0.6% (3/501 anomalies), in cases MDB21, MDB472, MDB481
absence of radius, bilateral 0.6% (3/501 anomalies), in cases MDB40, MDB265, MDB330
Single transverse palmar crease, unilateral 0.6% (3/501 anomalies), in cases MDB136, MDB397, MDB270
Nonimmune hydrops fetalis (NIHF) 0.6% (3/501 anomalies), in cases MDB339, MDB168, MDB481
Cystic hygroma 0.6% (3/501 anomalies), in cases MDB168, MDB391, MDB430
Cleft palate, bilateral 0.6% (3/501 anomalies), in cases MDB168, MDB332, MDB481
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.6% (3/501 anomalies), in cases MDB332, MDB358, MDB543
Syndactyly of the fingers, complex, bilateral 0.6% (3/501 anomalies), in cases MDB332, MDB358, MDB402
Renal agenesis, unilateral 0.6% (3/501 anomalies), in cases MDB358, MDB481, MDB503
Omphalocele 0.6% (3/501 anomalies), in cases MDB359, MDB487, MDB100
Dextrocardia, isolated 0.6% (3/501 anomalies), in cases MDB367, MDB391, MDB437
Corpus callosum agenesis 0.6% (3/501 anomalies), in cases MDB394, MDB438, MDB481
Long philtrum 0.6% (3/501 anomalies), in cases MDB397, MDB518, MDB270
Pulmonary artery hypoplasia 0.6% (3/501 anomalies), in cases MDB400, MDB481, MDB504
Dextroposition of aorta 0.6% (3/501 anomalies), in cases MDB400, MDB481, MDB504
Renal agenesis, bilateral 0.6% (3/501 anomalies), in cases MDB402, MDB438, MDB518
Microcephaly 0.4% (2/501 anomalies), in cases MDB21, MDB430
Ulna,absence of, bilateral 0.4% (2/501 anomalies), in cases MDB40, MDB265
Limbs hypoplasia 0.4% (2/501 anomalies), in cases MDB50, MDB471
Pulmonary artery dilatation, fetal 0.4% (2/501 anomalies), in cases MDB136, MDB332
Multicystic renal dysplasia,bilateral 0.4% (2/501 anomalies), in cases MDB255, MDB262
Bladder dilatation, fetal 0.4% (2/501 anomalies), in cases MDB255, MDB394
Cloacal dysgenesis sequence (CDS) 0.4% (2/501 anomalies), in cases MDB255, MDB262
Hepatomegaly, fetal 0.4% (2/501 anomalies), in cases MDB279, MDB524
Syndactyly of the toes, complex, bilateral 0.4% (2/501 anomalies), in cases MDB332, MDB431
Placental hypermaturity 0.4% (2/501 anomalies), in cases MDB332, MDB262
Retroplacental hemorrhage 0.4% (2/501 anomalies), in cases MDB368, MDB543
Malformed ear 0.4% (2/501 anomalies), in cases MDB359, MDB431
Preauricular hamartoma 0.4% (2/501 anomalies), in cases MDB391, MDB391
Ventricular septal defect, muscular 0.4% (2/501 anomalies), in cases MDB391, MDB399
Hypospadias, penile 0.4% (2/501 anomalies), in cases MDB394, MDB262
Hydrocephalus 0.4% (2/501 anomalies), in cases MDB394, MDB100
Tetralogy of Fallot 0.4% (2/501 anomalies), in cases MDB400, MDB504
Ureter agenesis, bilateral 0.4% (2/501 anomalies), in cases MDB402, MDB438
Cleft palate, median posterior 0.4% (2/501 anomalies), in cases MDB431, MDB518
Single cerebral ventricule 0.4% (2/501 anomalies), in cases MDB436, MDB438
Thalamic nuclei centrum medianum fusion 0.4% (2/501 anomalies), in cases MDB436, MDB161
Palpebral edema, bilateral 0.4% (2/501 anomalies), in cases MDB438, MDB472
Bladder hypoplasia 0.4% (2/501 anomalies), in cases MDB438, MDB503
Probst bundle 0.4% (2/501 anomalies), in cases MDB438, MDB481
Ventricular septal defect, membranous 0.4% (2/501 anomalies), in cases MDB470, MDB506
Renal hypoplasia, unilateral 0.4% (2/501 anomalies), in cases MDB481, MDB262
Thymic hypoplasia 0.4% (2/501 anomalies), in cases MDB481, MDB518
Communicating hydrocephalus 0.2% (1/501 anomalies), in case MDB21
Flattened occiput 0.2% (1/501 anomalies), in case MDB40
Oligodactyly 0.2% (1/501 anomalies), in case MDB40
Cornélia de Lange syndrome 0.2% (1/501 anomalies), in case MDB40
short nose 0.2% (1/501 anomalies), in case MDB40
Hitchhiker thumb 0.2% (1/501 anomalies), in case MDB50
Bowing of long bones of leg, congenital 0.2% (1/501 anomalies), in case MDB50
Dislocation of the radial head, congenital 0.2% (1/501 anomalies), in case MDB50
Diastrophic Dysplasia 0.2% (1/501 anomalies), in case MDB50
Flexion contracture of the fingers 0.2% (1/501 anomalies), in case MDB114
Polyhydramnios 0.2% (1/501 anomalies), in case MDB114
Akinesia, fetal 0.2% (1/501 anomalies), in case MDB114
Aortic valve stenosis, congenital 0.2% (1/501 anomalies), in case MDB136
Defective developement of left ventricle 0.2% (1/501 anomalies), in case MDB136
Right ventricle dilatation 0.2% (1/501 anomalies), in case MDB136
Right atrium Enlargement 0.2% (1/501 anomalies), in case MDB136
Polydactyly of both fingers & toes, postaxial 0.2% (1/501 anomalies), in case MDB136
Meckel diverticulum 0.2% (1/501 anomalies), in case MDB136
Renal hypoplasia, bilateral 0.2% (1/501 anomalies), in case MDB339
Hypoplasia of the liver 0.2% (1/501 anomalies), in case MDB168
Hexadactyly, postaxial 0.2% (1/501 anomalies), in case MDB168
Left ventricular hypertrophy, 0.2% (1/501 anomalies), in case MDB178
Epicanthus 0.2% (1/501 anomalies), in case MDB178
long straight nose 0.2% (1/501 anomalies), in case MDB178
Macrosomia 0.2% (1/501 anomalies), in case MDB255
Dilatation of ureter , bilateral, congenital 0.2% (1/501 anomalies), in case MDB255
Megarectum 0.2% (1/501 anomalies), in case MDB255
Thumb agenesis, bilateral 0.2% (1/501 anomalies), in case MDB265
Sloping forehead 0.2% (1/501 anomalies), in case MDB279
Thumb hypoplasia, bilateral 0.2% (1/501 anomalies), in case MDB330
Aortic valve atresia 0.2% (1/501 anomalies), in case MDB332
Exophthalmos, bilateral 0.2% (1/501 anomalies), in case MDB358
Aglossia 0.2% (1/501 anomalies), in case MDB358
Unilobate lung, bilateral 0.2% (1/501 anomalies), in case MDB358
Dermoid cyst of the ovary 0.2% (1/501 anomalies), in case MDB358
Hypogenesis of the Cerebellar Vermis 0.2% (1/501 anomalies), in case MDB359
Thin upper lip 0.2% (1/501 anomalies), in case MDB360
Diaphragmatic hernia,unilateral 0.2% (1/501 anomalies), in case MDB367
Dilatation of the ascending aorta, congenital 0.2% (1/501 anomalies), in case MDB367
Anotia 0.2% (1/501 anomalies), in case MDB391
Absence of diaphragm, left 0.2% (1/501 anomalies), in case MDB391
Pterygium colli 0.2% (1/501 anomalies), in case MDB391
Pectus excavatum 0.2% (1/501 anomalies), in case MDB391
Renal pelvis dilatation, bilateral 0.2% (1/501 anomalies), in case MDB394
Ureter hypoplasia 0.2% (1/501 anomalies), in case MDB394
Stenosis of the mid ureter, congenital, left side 0.2% (1/501 anomalies), in case MDB394
Hand edema 0.2% (1/501 anomalies), in case MDB394
Foot edema 0.2% (1/501 anomalies), in case MDB394
Arnold-Chiari Type II malformation (CM II) 0.2% (1/501 anomalies), in case MDB397
Myelomeningocele, lumbosacral 0.2% (1/501 anomalies), in case MDB397
Right ventricular hypoplasia 0.2% (1/501 anomalies), in case MDB400
Cleft palate with cleft lip,bilateral, complete 0.2% (1/501 anomalies), in case MDB402
Fraser syndrome 0.2% (1/501 anomalies), in case MDB402
Subglottic Stenosis (CSS) 0.2% (1/501 anomalies), in case MDB402
Non-segmented lung 0.2% (1/501 anomalies), in case MDB402
Bladder agenesis 0.2% (1/501 anomalies), in case MDB402
Left side appendix 0.2% (1/501 anomalies), in case MDB402
Micropenis 0.2% (1/501 anomalies), in case MDB402
Pyloric stenosis 0.2% (1/501 anomalies), in case MDB402
Amnion nodosum 0.2% (1/501 anomalies), in case MDB402
Radial ray agenesis, unilateral 0.2% (1/501 anomalies), in case MDB431
Thumb hypoplasia,unilateral 0.2% (1/501 anomalies), in case MDB431
Wide space between 2nd and third fingers 0.2% (1/501 anomalies), in case MDB431
Dislocation of hip, unilateral 0.2% (1/501 anomalies), in case MDB431
Scaphoid abdomen 0.2% (1/501 anomalies), in case MDB431
Absence of neuron differentiation in the basal nuclei. 0.2% (1/501 anomalies), in case MDB436
Nasal Clefts 0.2% (1/501 anomalies), in case MDB437
Absence of Anterior Commissure 0.2% (1/501 anomalies), in case MDB438
Incomplete cleavage of cerebral hemispheres 0.2% (1/501 anomalies), in case MDB438
Uterus agenesis 0.2% (1/501 anomalies), in case MDB438
Fallopian tube, absence of 0.2% (1/501 anomalies), in case MDB438
small intestinal atresia and stenosis 0.2% (1/501 anomalies), in case MDB456
Pleural effusion, fetal 0.2% (1/501 anomalies), in case MDB456
Micro Multicystic kidneys, medullary type 0.2% (1/501 anomalies), in case MDB456
Mucus accumulation in small intestine. 0.2% (1/501 anomalies), in case MDB466
Frontal bossing 0.2% (1/501 anomalies), in case MDB471
Flat face 0.2% (1/501 anomalies), in case MDB472
Oligohydramnios 0.2% (1/501 anomalies), in case MDB472
Ambiguous genitalia 0.2% (1/501 anomalies), in case MDB481
Rocker-bottom feet 0.2% (1/501 anomalies), in case MDB481
Persistent left superior vena cava 0.2% (1/501 anomalies), in case MDB481
Presence of an infantile uterus with both testes 0.2% (1/501 anomalies), in case MDB481
Absence of the Septum Pellucidum 0.2% (1/501 anomalies), in case MDB481
Cerebral ventriculomegaly 0.2% (1/501 anomalies), in case MDB481
Trilobate lung, bilateral 0.2% (1/501 anomalies), in case MDB487
Flexion contracture of upper limbs 0.2% (1/501 anomalies), in case MDB503
Renal ectopia,crossed 0.2% (1/501 anomalies), in case MDB503
Ureter agenesis, unilateral 0.2% (1/501 anomalies), in case MDB503
Dysplastic kidney with tubular cysts 0.2% (1/501 anomalies), in case MDB503
Bicornuate uterus 0.2% (1/501 anomalies), in case MDB503
Cleft palate with cleft lip (CLP), median 0.2% (1/501 anomalies), in case MDB504
Cutaneous bud 0.2% (1/501 anomalies), in case MDB504
Hypotelorisme 0.2% (1/501 anomalies), in case MDB504
Aplasia cutis congenita, scalp 0.2% (1/501 anomalies), in case MDB504
Camptodactyly, bilateral 0.2% (1/501 anomalies), in case MDB504
Pulmonary valve atresia 0.2% (1/501 anomalies), in case MDB504
Right ventricular hypertrophy 0.2% (1/501 anomalies), in case MDB504
Hypoplasia of diaphragm 0.2% (1/501 anomalies), in case MDB506
Lumbosacral agenesis 0.2% (1/501 anomalies), in case MDB518
Relative Macrocephaly 0.2% (1/501 anomalies), in case MDB518
Agenesia of internal genital organs 0.2% (1/501 anomalies), in case MDB518
Persistent truncus arteriosus 0.2% (1/501 anomalies), in case MDB518
Right aortic arch 0.2% (1/501 anomalies), in case MDB518
Right bilobate lung 0.2% (1/501 anomalies), in case MDB518
Unilobate lung, unilateral 0.2% (1/501 anomalies), in case MDB518
Gastroschisis 0.2% (1/501 anomalies), in case MDB518
Rachischisis 0.2% (1/501 anomalies), in case MDB518
Vertebral hypoplasia, dorsolumbar 0.2% (1/501 anomalies), in case MDB518
Rib deformation with abnormal numbers, bilateral 0.2% (1/501 anomalies), in case MDB518
Underdeveloped pelvic bones 0.2% (1/501 anomalies), in case MDB518
Long umbilical cord 0.2% (1/501 anomalies), in case MDB524
Marginal subchorionic hematoma 0.2% (1/501 anomalies), in case MDB524
Splenomegaly, congenital 0.2% (1/501 anomalies), in case MDB524
Arthrogryposis 0.2% (1/501 anomalies), in case MDB543
Large nose, fetal 0.2% (1/501 anomalies), in case MDB543
Macrostomia 0.2% (1/501 anomalies), in case MDB543
Large ear, fetal 0.2% (1/501 anomalies), in case MDB90
Cubital pterygium, bilateral 0.2% (1/501 anomalies), in case MDB90
Cubital deviation of the hand, unilateral 0.2% (1/501 anomalies), in case MDB90
Radial deviation of the hand, unilateral 0.2% (1/501 anomalies), in case MDB90
Autosomal Recessive Polycystic Kidney Disease 0.2% (1/501 anomalies), in case MDB146
Nephromegaly, bilateral 0.2% (1/501 anomalies), in case MDB146
Renal-hepatic-pancreatic dysplasia 0.2% (1/501 anomalies), in case MDB146
Renal pelvis dilatation, unilateral 0.2% (1/501 anomalies), in case MDB146
Olfactory nerve, absence of, bilateral 0.2% (1/501 anomalies), in case MDB161
Trigonocephaly 0.2% (1/501 anomalies), in case MDB161
Olfactory bulbs, absence of 0.2% (1/501 anomalies), in case MDB161
Holoprosencephaly 0.2% (1/501 anomalies), in case MDB161
Duodenal atresia and stenosis, congenital 0.2% (1/501 anomalies), in case MDB262
Rectovesical fistula 0.2% (1/501 anomalies), in case MDB262
Crossed fused renal ectopia 0.2% (1/501 anomalies), in case MDB262
Hydronephrosis, congenital, unilateral 0.2% (1/501 anomalies), in case MDB262
Hydroureter, unilateral 0.2% (1/501 anomalies), in case MDB262
Polysplenia 0.2% (1/501 anomalies), in case MDB262
Micrognathia 0.2% (1/501 anomalies), in case MDB262
Pulmonary lobation anomalies 0.2% (1/501 anomalies), in case MDB262
Macroglossia 0.2% (1/501 anomalies), in case MDB270
Diaphragmatic hernia, congenital 0.2% (1/501 anomalies), in case MDB100
Renal focal cystic dilatation of collecting tubules 0.2% (1/501 anomalies), in case MDB100

Terminology and coding

References

No reference related to Retrognathia is available at the moment.

Last modified: 2008-12-05 17:05:33 by farideh

Created: 2008-02-26 00:00:00 by phsaw

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