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Micrognathia

DA: 419

Developmental anomaly information

Definition: Micrognathia is a relative term describing the small size of the lower jaw.

Synonyms:

mandibular hypoplasia
congenital micrognathia micrognathism

Developmental anomaly parent: (empty)	Topology: Human body > Head and neck > Head > Face
System: Human body > musculoskeletal system. > Bones	Developmental anomaly category: Anomaly of underdevelopment or overdevelopment

Case records MDB9, MDB17, MDB48, MDB78, MDB104, MDB134, MDB145, MDB157, MDB172, MDB196, MDB200, MDB60, MDB207, MDB209, MDB216, MDB217, MDB229, MDB230, MDB236, MDB238, MDB240, MDB242, MDB263, MDB274, MDB286, MDB287, MDB291, MDB305, MDB314, MDB310, MDB312, MDB363, MDB364, MDB365, MDB374, MDB378, MDB380, MDB404, MDB412, MDB448, MDB467, MDB473, MDB479, MDB489, MDB500, MDB501, MDB508, MDB171, MDB257, MDB262, MDB302, MDB101, MDB107, MDB315, MDB317, MDB320, MDB324

Links

Humpath: 4552

Observed in MDB cases

In malformative diseases :

Cousin syndrome

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in case 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 5.02% (29/578 anomalies), in cases MDB9, MDB17, MDB48, MDB104, MDB134, MDB145, MDB172, MDB200, MDB216, MDB217, MDB238, MDB240, MDB263, MDB286, MDB314, MDB312, MDB374, MDB378, MDB448, MDB467, MDB473, MDB479, MDB171, MDB257, MDB101, MDB107, MDB315, MDB317, MDB320
Low-set ears 3.63% (21/578 anomalies), in cases MDB9, MDB17, MDB48, MDB134, MDB196, MDB60, MDB209, MDB216, MDB217, MDB238, MDB242, MDB287, MDB310, MDB312, MDB380, MDB404, MDB473, MDB489, MDB171, MDB257, MDB101
Placenta hypoplasia 3.29% (19/578 anomalies), in cases MDB48, MDB157, MDB196, MDB200, MDB209, MDB242, MDB263, MDB274, MDB286, MDB287, MDB291, MDB305, MDB310, MDB473, MDB171, MDB101, MDB315, MDB317, MDB320
Pulmonary hypoplasia 2.77% (16/578 anomalies), in cases MDB9, MDB104, MDB200, MDB207, MDB209, MDB230, MDB236, MDB238, MDB274, MDB291, MDB380, MDB404, MDB171, MDB302, MDB107, MDB324
Intrauterine growth retardation, symmetric 2.77% (16/578 anomalies), in cases MDB236, MDB263, MDB274, MDB286, MDB291, MDB305, MDB314, MDB310, MDB378, MDB380, MDB404, MDB467, MDB473, MDB489, MDB302, MDB101
Hypertelorism 2.6% (15/578 anomalies), in cases MDB104, MDB145, MDB196, MDB207, MDB217, MDB238, MDB240, MDB363, MDB374, MDB448, MDB473, MDB479, MDB257, MDB315, MDB320
Talipes equinovarus, bilateral 1.73% (10/578 anomalies), in cases MDB104, MDB209, MDB238, MDB274, MDB310, MDB363, MDB479, MDB257, MDB317, MDB324
Lobulated, fused and horseshoe kidney 1.56% (9/578 anomalies), in cases MDB48, MDB157, MDB310, MDB364, MDB380, MDB257, MDB262, MDB101, MDB320
Flattened nose 1.56% (9/578 anomalies), in cases MDB104, MDB207, MDB209, MDB236, MDB263, MDB467, MDB500, MDB320, MDB324
Clindodactyly of 5th finger, bilateral 1.38% (8/578 anomalies), in cases MDB48, MDB145, MDB196, MDB200, MDB217, MDB107, MDB315, MDB324
Low nasal bridge 1.21% (7/578 anomalies), in cases MDB9, MDB145, MDB172, MDB207, MDB287, MDB305, MDB324
Microcephaly 1.21% (7/578 anomalies), in cases MDB17, MDB104, MDB60, MDB263, MDB291, MDB473, MDB315
Coarctation of aorta, 1.21% (7/578 anomalies), in cases MDB157, MDB236, MDB286, MDB489, MDB262, MDB302, MDB101
Long philtrum 1.21% (7/578 anomalies), in cases MDB172, MDB378, MDB467, MDB508, MDB257, MDB320, MDB324
Toe hypoplasia, first, bilateral 1.21% (7/578 anomalies), in cases MDB242, MDB263, MDB314, MDB310, MDB448, MDB489, MDB302
Neck edema 1.04% (6/578 anomalies), in cases MDB17, MDB200, MDB263, MDB310, MDB404, MDB324
Broad nasal bridge 1.04% (6/578 anomalies), in cases MDB48, MDB104, MDB196, MDB207, MDB107, MDB320
Short neck 1.04% (6/578 anomalies), in cases MDB172, MDB363, MDB374, MDB467, MDB479, MDB320
Wide space between 1st and 2nd toes, bilateral 1.04% (6/578 anomalies), in cases MDB196, MDB216, MDB287, MDB305, MDB302, MDB107
Prominent and pointed nose 1.04% (6/578 anomalies), in cases MDB216, MDB217, MDB242, MDB286, MDB378, MDB317
Single umblical artery (SUA)-Isolated 0.87% (5/578 anomalies), in cases MDB9, MDB209, MDB448, MDB501, MDB262
Potter deformity sequence 0.87% (5/578 anomalies), in cases MDB104, MDB207, MDB209, MDB500, MDB324
Bladder hypoplasia 0.87% (5/578 anomalies), in cases MDB104, MDB207, MDB209, MDB310, MDB374
Microstomia 0.87% (5/578 anomalies), in cases MDB157, MDB172, MDB291, MDB305, MDB320
Posteriorly inclined and low-positioned ears 0.87% (5/578 anomalies), in cases MDB172, MDB479, MDB501, MDB320, MDB324
Adrenal hypoplasia, fetal 0.87% (5/578 anomalies), in cases MDB196, MDB286, MDB380, MDB404, MDB302
Macroglossia 0.69% (4/578 anomalies), in cases MDB17, MDB145, MDB200, MDB171
Retroplacental hemorrhage 0.69% (4/578 anomalies), in cases MDB134, MDB364, MDB365, MDB324
Cerebral ventriculomegaly 0.69% (4/578 anomalies), in cases MDB145, MDB172, MDB60, MDB217
Overlapping fingers 0.69% (4/578 anomalies), in cases MDB157, MDB238, MDB489, MDB101
Ventricular septal defect, muscular 0.69% (4/578 anomalies), in cases MDB157, MDB412, MDB257, MDB101
Gothic palate 0.69% (4/578 anomalies), in cases MDB172, MDB263, MDB479, MDB320
Renal hypoplasia 0.69% (4/578 anomalies), in cases MDB196, MDB287, MDB374, MDB171
Cerebellar hypoplasia 0.69% (4/578 anomalies), in cases MDB60, MDB291, MDB310, MDB315
Potter's facies 0.69% (4/578 anomalies), in cases MDB207, MDB209, MDB500, MDB324
Arthrogryposis 0.69% (4/578 anomalies), in cases MDB230, MDB238, MDB479, MDB257
Renal pelvis dilatation, bilateral 0.69% (4/578 anomalies), in cases MDB489, MDB500, MDB320, MDB324
Epicanthus 0.52% (3/578 anomalies), in cases MDB134, MDB200, MDB217
Transverse palmar crease, bilateral 0.52% (3/578 anomalies), in cases MDB134, MDB363, MDB448
Aberrant right subclavian artery 0.52% (3/578 anomalies), in cases MDB145, MDB209, MDB404
Narrow thorax 0.52% (3/578 anomalies), in cases MDB196, MDB286, MDB467
Syndactyly of the feet , simple (webbed), unilateral 0.52% (3/578 anomalies), in cases MDB196, MDB310, MDB101
Polydactyly of the hand, preaxial 0.52% (3/578 anomalies), in cases MDB60, MDB380, MDB473
Clindodactyly of 5th finger, unilateral 0.52% (3/578 anomalies), in cases MDB216, MDB287, MDB305
Single transverse palmar crease, unilateral 0.52% (3/578 anomalies), in cases MDB230, MDB242, MDB305
Long umbilical cord 0.52% (3/578 anomalies), in cases MDB236, MDB291, MDB310
Single cerebral ventricule 0.52% (3/578 anomalies), in cases MDB263, MDB291, MDB473
Corpus callosum agenesis 0.52% (3/578 anomalies), in cases MDB263, MDB291, MDB473
Brachydactyly 0.52% (3/578 anomalies), in cases MDB274, MDB287, MDB305
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.52% (3/578 anomalies), in cases MDB286, MDB380, MDB171
Syndactyly of the fingers, complex, unilateral 0.52% (3/578 anomalies), in cases MDB286, MDB380, MDB302
Large nose, fetal 0.52% (3/578 anomalies), in cases MDB312, MDB448, MDB171
Thin upper lip 0.52% (3/578 anomalies), in cases MDB378, MDB508, MDB320
Syndactyly of the toes, unilateral 0.52% (3/578 anomalies), in cases MDB380, MDB467, MDB171
Hydronephrosis, congenital, bilateral 0.52% (3/578 anomalies), in cases MDB489, MDB500, MDB320
Megacystis 0.52% (3/578 anomalies), in cases MDB500, MDB320, MDB324
Dilatation of ureter , bilateral, congenital 0.52% (3/578 anomalies), in cases MDB500, MDB320, MDB324
Ascites, fetal 0.35% (2/578 anomalies), in cases MDB9, MDB324
Scoliosis, congenital 0.35% (2/578 anomalies), in cases MDB9, MDB238
Infarcted placenta 0.35% (2/578 anomalies), in cases MDB134, MDB236
Mongoloid slope of the palpebral fissures 0.35% (2/578 anomalies), in cases MDB145, MDB200
Right bilobate lung 0.35% (2/578 anomalies), in cases MDB145, MDB196
Meckel diverticulum 0.35% (2/578 anomalies), in cases MDB157, MDB101
Flattened occiput 0.35% (2/578 anomalies), in cases MDB172, MDB107
Limbs hypoplasia 0.35% (2/578 anomalies), in cases MDB172, MDB274
Frontal bossing 0.35% (2/578 anomalies), in cases MDB196, MDB257
Short philtrum 0.35% (2/578 anomalies), in cases MDB196, MDB473
Intrauterine growth retardation, asymmetric 0.35% (2/578 anomalies), in cases MDB196, MDB312
Rocker-bottom feet 0.35% (2/578 anomalies), in cases MDB196, MDB479
Sloping forehead 0.35% (2/578 anomalies), in cases MDB200, MDB324
Nasal hypoplasia 0.35% (2/578 anomalies), in cases MDB200, MDB263
Semilobar holoprosencephaly 0.35% (2/578 anomalies), in cases MDB60, MDB473
Badly-hemmed ears 0.35% (2/578 anomalies), in cases MDB60, MDB320
Microtia 0.35% (2/578 anomalies), in cases MDB60, MDB467
Macrocephaly 0.35% (2/578 anomalies), in cases MDB60, MDB217
Hydrocephalus 0.35% (2/578 anomalies), in cases MDB60, MDB217
Hypogenesis of the Cerebellar Vermis 0.35% (2/578 anomalies), in cases MDB60, MDB310
Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.35% (2/578 anomalies), in cases MDB60, MDB473
Renal agenesis, bilateral 0.35% (2/578 anomalies), in cases MDB207, MDB209
Ureter agenesis, bilateral 0.35% (2/578 anomalies), in cases MDB207, MDB209
Prostate hypoplasia 0.35% (2/578 anomalies), in cases MDB207, MDB209
Imperforate Anus 0.35% (2/578 anomalies), in cases MDB209, MDB262
Pericardial effusion 0.35% (2/578 anomalies), in cases MDB209, MDB324
Syndactyly, simple (webbed), fingers 0.35% (2/578 anomalies), in cases MDB238, MDB286
Cleft palate, bilateral 0.35% (2/578 anomalies), in cases MDB238, MDB257
Holoprosencephaly, lobar 0.35% (2/578 anomalies), in cases MDB263, MDB291
Thalamic nuclei centrum medianum fusion 0.35% (2/578 anomalies), in cases MDB263, MDB291
Exophthalmos, bilateral 0.35% (2/578 anomalies), in cases MDB263, MDB286
Triangular face 0.35% (2/578 anomalies), in cases MDB314, MDB317
Ventricular septal defect, membranous 0.35% (2/578 anomalies), in cases MDB310, MDB404
Cubital deviation of the hand, unilateral 0.35% (2/578 anomalies), in cases MDB364, MDB479
Hydronephrosis, congenital, unilateral 0.35% (2/578 anomalies), in cases MDB374, MDB262
Myelomeningocele, lumbosacral 0.35% (2/578 anomalies), in cases MDB378, MDB412
Cleft palate, median posterior 0.35% (2/578 anomalies), in cases MDB467, MDB320
Polydactyly,of the hand, postaxial 0.35% (2/578 anomalies), in cases MDB473, MDB501
Small mouth 0.35% (2/578 anomalies), in cases MDB479, MDB257
Nonimmune hydrops fetalis (NIHF) 0.35% (2/578 anomalies), in cases MDB479, MDB257
Posterior urethral valves, congenital 0.35% (2/578 anomalies), in cases MDB500, MDB320
Hydroureter, unilateral 0.35% (2/578 anomalies), in cases MDB501, MDB262
Stenosis of aqueduct of Sylvius 0.35% (2/578 anomalies), in cases MDB257, MDB315
Multicystic renal dysplasia,bilateral 0.35% (2/578 anomalies), in cases MDB262, MDB320
Omphalocele 0.17% (1/578 anomalies), in case MDB9
Varus deviation of fingers 0.17% (1/578 anomalies), in case MDB9
Communicating hydrocephalus 0.17% (1/578 anomalies), in case MDB17
Pes cavus 0.17% (1/578 anomalies), in case MDB48
Multiple pterygium 0.17% (1/578 anomalies), in case MDB78
Encephalocele, occipital 0.17% (1/578 anomalies), in case MDB104
Nephromegaly, bilateral 0.17% (1/578 anomalies), in case MDB104
Autosomal Recessive Polycystic Kidney Disease 0.17% (1/578 anomalies), in case MDB104
Renal-hepatic-pancreatic dysplasia 0.17% (1/578 anomalies), in case MDB104
Hexadactyly, postaxial 0.17% (1/578 anomalies), in case MDB104
Ureter hypoplasia 0.17% (1/578 anomalies), in case MDB104
Dolicocephaly 0.17% (1/578 anomalies), in case MDB134
Periventricular Leukomalacia (PVL) 0.17% (1/578 anomalies), in case MDB134
Flat face 0.17% (1/578 anomalies), in case MDB145
Turricephaly 0.17% (1/578 anomalies), in case MDB172
Hypotelorisme 0.17% (1/578 anomalies), in case MDB172
Camptodactyly, bilateral 0.17% (1/578 anomalies), in case MDB172
Plantar vertical crease between 1st and 2nd toes, bilateral 0.17% (1/578 anomalies), in case MDB172
Aortic valve stenosis, congenital 0.17% (1/578 anomalies), in case MDB172
Wide spaced hypoplastic nipples 0.17% (1/578 anomalies), in case MDB172
Arachnodactyly of the toes 0.17% (1/578 anomalies), in case MDB196
5th toe hypoplasia 0.17% (1/578 anomalies), in case MDB196
Relative Macrocephaly 0.17% (1/578 anomalies), in case MDB196
Bulbous nose 0.17% (1/578 anomalies), in case MDB196
Micropenis 0.17% (1/578 anomalies), in case MDB196
Hand clenching, fetal 0.17% (1/578 anomalies), in case MDB196
Flexion contracture of the fingers 0.17% (1/578 anomalies), in case MDB196
Arachnodactyly 0.17% (1/578 anomalies), in case MDB196
Short and dorsiflexed great toe 0.17% (1/578 anomalies), in case MDB196
Abnormally aligned ribs 0.17% (1/578 anomalies), in case MDB196
Recessed forehead 0.17% (1/578 anomalies), in case MDB200
Large anterior fontanelle 0.17% (1/578 anomalies), in case MDB60
Cleft palate with cleft lip (CLP), median 0.17% (1/578 anomalies), in case MDB60
Preauricular hamartoma 0.17% (1/578 anomalies), in case MDB60
Cryptophthalmos 0.17% (1/578 anomalies), in case MDB60
Flexion contracture of upper limbs 0.17% (1/578 anomalies), in case MDB60
Dysplastic kidney with tubular cysts 0.17% (1/578 anomalies), in case MDB60
absence of nasal septum 0.17% (1/578 anomalies), in case MDB60
Hypoplasia of eye 0.17% (1/578 anomalies), in case MDB60
skin hamartoma 0.17% (1/578 anomalies), in case MDB60
Aqueduct of Sylvius atresia 0.17% (1/578 anomalies), in case MDB60
Cerebral commissures agenesis 0.17% (1/578 anomalies), in case MDB60
Talipes calcaneovalgus 0.17% (1/578 anomalies), in case MDB207
Prominent infraorbital creases 0.17% (1/578 anomalies), in case MDB207
Persistent left superior vena cava 0.17% (1/578 anomalies), in case MDB209
Prominence of nasofrontal angle 0.17% (1/578 anomalies), in case MDB217
Defective developement of left ventricle 0.17% (1/578 anomalies), in case MDB229
Mitral valve atresia 0.17% (1/578 anomalies), in case MDB229
Aortic atresia 0.17% (1/578 anomalies), in case MDB229
Axillary pterygia, bilateral 0.17% (1/578 anomalies), in case MDB238
Renal hypertropy, fetal, bilateral 0.17% (1/578 anomalies), in case MDB238
Dextrocardia, isolated 0.17% (1/578 anomalies), in case MDB240
Endocardial fibroelastosis 0.17% (1/578 anomalies), in case MDB240
Absence of first finger, unilateral 0.17% (1/578 anomalies), in case MDB263
Fissure of the upper gingiva, fetal 0.17% (1/578 anomalies), in case MDB263
Diastrophic Dysplasia 0.17% (1/578 anomalies), in case MDB274
Bowing of long bones 0.17% (1/578 anomalies), in case MDB274
Cubital deviation of the hand, bilateral 0.17% (1/578 anomalies), in case MDB274
Hypoplasia of optic nerve, bilateral 0.17% (1/578 anomalies), in case MDB291
Olfactory bulbs, absence of 0.17% (1/578 anomalies), in case MDB291
Olfactory nerve, absence of, bilateral 0.17% (1/578 anomalies), in case MDB291
Arhinencephaly 0.17% (1/578 anomalies), in case MDB291
Anophthalmos, bilateral 0.17% (1/578 anomalies), in case MDB291
Arhinia 0.17% (1/578 anomalies), in case MDB291
Trigonocephaly 0.17% (1/578 anomalies), in case MDB291
Cyclopia 0.17% (1/578 anomalies), in case MDB291
Absence of neocortex 0.17% (1/578 anomalies), in case MDB291
Absence of the pyramid tracts, bilateral 0.17% (1/578 anomalies), in case MDB291
Wide space between 4th and 5th toes, unilateral 0.17% (1/578 anomalies), in case MDB312
Foot valgus 0.17% (1/578 anomalies), in case MDB312
Talipes equinovarus,unilateral 0.17% (1/578 anomalies), in case MDB364
Ureter stenosis, proximal, unilateral 0.17% (1/578 anomalies), in case MDB374
Renal pelvis dilatation, unilateral 0.17% (1/578 anomalies), in case MDB374
Hand edema 0.17% (1/578 anomalies), in case MDB374
Arnold-Chiari Type II malformation (CM II) 0.17% (1/578 anomalies), in case MDB378
Limbs hypoplasia, lower extremities 0.17% (1/578 anomalies), in case MDB378
Toe hypoplasia, unilateral 0.17% (1/578 anomalies), in case MDB380
Pulmonary artery hypoplasia 0.17% (1/578 anomalies), in case MDB380
Renal focal cystic dilatation of collecting tubules 0.17% (1/578 anomalies), in case MDB380
left carotid artery, aberrant 0.17% (1/578 anomalies), in case MDB404
Acrocephaly 0.17% (1/578 anomalies), in case MDB448
Overlapping toes 0.17% (1/578 anomalies), in case MDB448
Placenta villous fibrosis 0.17% (1/578 anomalies), in case MDB448
Otopaladigital syndrome, Type II; 0.17% (1/578 anomalies), in case MDB467
Tetra-amelia 0.17% (1/578 anomalies), in case MDB467
Polydactyly postaxial & preaxial of toes 0.17% (1/578 anomalies), in case MDB467
Thumb malformation & mal-implanted 0.17% (1/578 anomalies), in case MDB467
Anotia 0.17% (1/578 anomalies), in case MDB467
Choanal Atresia 0.17% (1/578 anomalies), in case MDB467
Incomplete cleavage of cerebral hemispheres 0.17% (1/578 anomalies), in case MDB473
Myelomeningocele,thoracolumbar 0.17% (1/578 anomalies), in case MDB473
Giant omphalocele 0.17% (1/578 anomalies), in case MDB473
hypoplasia of the rib 0.17% (1/578 anomalies), in case MDB473
Pulmonary valve dysplasia 0.17% (1/578 anomalies), in case MDB473
Tricuspid valve dysplasia 0.17% (1/578 anomalies), in case MDB473
Interauricular communication 0.17% (1/578 anomalies), in case MDB473
Pena Shokeir syndrome , Type I 0.17% (1/578 anomalies), in case MDB479
Placental hydrops 0.17% (1/578 anomalies), in case MDB479
Ureterovesical junction stenosis 0.17% (1/578 anomalies), in case MDB489
Penis edema 0.17% (1/578 anomalies), in case MDB500
Intra-abdominal testicule 0.17% (1/578 anomalies), in case MDB500
Mandibulofacial dysostosis 0.17% (1/578 anomalies), in case MDB501
Polydactyly of the foot 0.17% (1/578 anomalies), in case MDB501
Split-hand/split-foot malformation (SHFM) 0.17% (1/578 anomalies), in case MDB501
Renal agenesis, unilateral 0.17% (1/578 anomalies), in case MDB501
Ureter agenesis, unilateral 0.17% (1/578 anomalies), in case MDB501
Unicorn Uterus 0.17% (1/578 anomalies), in case MDB501
Acro–renal–mandibular syndrome 0.17% (1/578 anomalies), in case MDB501
Wide space between 1st and 2nd toes, unilateral 0.17% (1/578 anomalies), in case MDB508
Hypoplasia of ascending aorta 0.17% (1/578 anomalies), in case MDB508
Transverse aortic hypoplasia 0.17% (1/578 anomalies), in case MDB508
Syndactyly of the fingers, complex, bilateral 0.17% (1/578 anomalies), in case MDB171
Dysplasia of deep nuclei (olive dysplasia) 0.17% (1/578 anomalies), in case MDB257
Hydrocephalus, Non-communicating 0.17% (1/578 anomalies), in case MDB257
Cystic hygroma 0.17% (1/578 anomalies), in case MDB257
Microphthalmia 0.17% (1/578 anomalies), in case MDB257
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.17% (1/578 anomalies), in case MDB257
Hypogenesis of pyramidal tracts 0.17% (1/578 anomalies), in case MDB257
Unilobate lung, bilateral 0.17% (1/578 anomalies), in case MDB257
Duodenal atresia and stenosis, congenital 0.17% (1/578 anomalies), in case MDB262
Cloacal dysgenesis sequence (CDS) 0.17% (1/578 anomalies), in case MDB262
Rectovesical fistula 0.17% (1/578 anomalies), in case MDB262
Crossed fused renal ectopia 0.17% (1/578 anomalies), in case MDB262
Renal hypoplasia, unilateral 0.17% (1/578 anomalies), in case MDB262
Hypospadias, penile 0.17% (1/578 anomalies), in case MDB262
Polysplenia 0.17% (1/578 anomalies), in case MDB262
Retrognathia 0.17% (1/578 anomalies), in case MDB262
Pulmonary lobation anomalies 0.17% (1/578 anomalies), in case MDB262
Placental hypermaturity 0.17% (1/578 anomalies), in case MDB262
Syndactyly of the feet , simple (webbed), bilateral 0.17% (1/578 anomalies), in case MDB101
Aortic valve atresia 0.17% (1/578 anomalies), in case MDB101
Turned-up nose 0.17% (1/578 anomalies), in case MDB101
Small round skull 0.17% (1/578 anomalies), in case MDB107
Trilobate lung, left 0.17% (1/578 anomalies), in case MDB107
Macrostomia 0.17% (1/578 anomalies), in case MDB315
Bladder wall thickness 0.17% (1/578 anomalies), in case MDB320
Hypospadias, Glandular 0.17% (1/578 anomalies), in case MDB320
Hypoplasia and dysplasia of the kidney, bilateral 0.17% (1/578 anomalies), in case MDB324
Pleural effusion, fetal 0.17% (1/578 anomalies), in case MDB324

Terminology and coding

References

No reference related to Micrognathia is available at the moment.

Last modified: 2009-05-04 19:17:42 by jcfournet

Created: 2008-06-18 18:31:40 by farideh

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