121:
1020:
113:
727:
58:
1279:
100:. It is common in infants, but is usually self-corrected during growth, due to the jaws' increasing in size. It may be a cause of abnormal tooth alignment and in severe cases can hamper feeding. It can also, both in adults and children, make
1595:
Hong, Paul; Brake, Maria K.; Cavanagh, Jonathan P.; Bezuhly, Michael; Magit, Anthony E. (2012). "Feeding and mandibular distraction osteogenesis in children with Pierre Robin sequence: A case series of functional outcomes".
1528:
Micrognathia can be treated by surgery and modified eating methods. Early detection of the problem and monitoring as the problems grows can help understand it better and find the most effective treatment procedure.
1698:
1683:
1414:
1568:
MartĂnez-FrĂas, ML; MartĂn, M; Pardo, M; Torres, M; Cohen MM, Jr (1993). "Holoprosencephaly and hypognathia with two proboscides: report of a case and review of unusual proboscides".
752:
1805:
1059:
1403:
1798:
991:
932:
1458:
1791:
975:
960:
179:
862:
438:
1313:
225:
204:
1184:
1168:
769:
362:
235:
997:
357:
284:
1951:
1443:
1408:
1179:
781:
758:
342:
246:
1195:
458:
420:
713:
1381:
1138:
852:
507:
230:
209:
66:
17:
1162:
1121:
876:
735:
699:
279:
145:
1490:
1392:
1319:
1256:
1174:
923:
541:
490:
473:
452:
1468:
1339:
1333:
215:
1713:
1495:
1484:
1364:
1223:
1144:
980:
908:
826:
386:
316:
257:
157:
125:
1463:
1397:
1386:
1262:
1150:
985:
837:
775:
764:
669:
652:
641:
629:
525:
496:
426:
220:
1972:
1301:
940:
902:
740:
606:
574:
327:
322:
306:
1768:
1753:
1452:
1228:
1065:
1053:
955:
885:
810:
694:
552:
433:
391:
352:
337:
184:
167:
1868:
1500:
1267:
896:
531:
8:
1702:
1296:
1156:
1103:
689:
623:
595:
311:
301:
276:
528:
1, 6, 10, 14 (with mandibulofacial dysostosis), 15 (with mandibulofacial dysostosis), 21
1900:
1707:
1359:
1291:
1199:
1094:
1080:
636:
380:
368:
294:
267:
1895:
1724:
1621:
1613:
1577:
1431:
1419:
1085:
950:
831:
719:
611:
569:
564:
547:
479:
140:
73:
1012:
Microcephaly 2, primary, autosomal recessive, with or without cortical malformations
1783:
1605:
1473:
1437:
1325:
1232:
1190:
746:
679:
586:
373:
347:
270:
78:
1905:
1832:
1718:
1609:
1370:
1272:
1132:
1115:
1037:
966:
945:
869:
857:
842:
821:
674:
663:
646:
513:
484:
162:
1814:
1729:
1538:
1376:
1250:
1127:
1071:
1031:
683:
600:
519:
415:
95:
1692:
1966:
1929:
1617:
1548:
1543:
1505:
1479:
1343:
1047:
1042:
915:
890:
881:
658:
120:
31:
1639:
1842:
1837:
1625:
1415:
Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
1241:
1019:
1003:
815:
794:
708:
1581:
112:
1924:
1748:
1245:
800:
617:
1675:
1109:
501:
332:
194:
101:
1939:
1890:
1847:
1400:, lower extremity-predominant, 2b, prenatal onset, autosomal dominant
704:
151:
594:, X-linked 2, with or without impaired intellectual development and
1944:
1882:
927:
804:
591:
537:
190:
753:
Immunodeficiency-centromeric instability-facial anomalies syndrome
1878:
104:
difficult, either during anesthesia or in emergency situations.
1687:
1567:
1517:
1516:
It can be detected by the naked eye as well as dental or skull
1349:
846:
558:
239:
1278:
1356:
1287:
726:
261:
57:
1425:
1307:
1217:
1076:
409:
403:
397:
200:
133:
1570:
1818:
1060:
Multiple congenital anomalies-hypotonia-seizures syndrome
90:
1594:
1023:
Micrognathism in microcephaly (with normal intelligence)
787:
Intellectual disability, X-linked syndromic, Turner type
1496:
X-linked intellectual disability with marfanoid habitus
1404:
Splenogonadal fusion-limb defects-micrognathia syndrome
790:
Intellectual disability, X-linked, syndromic, Bain type
245:
Arthrogryposis multiplex congenita 4, neurogenic, with
51:
Micrognathia, strawberry chin, hypognathia hypognathism
1598:
International
Journal of Pediatric Otorhinolaryngology
1028:
Microcephaly, normal intelligence and immunodeficiency
1813:
1665:
1449:
Syndromic X-linked intellectual disability Najm type
1411:
with joint laxity, type 1, with or without fractures
1253:
with or without vascular-type Ehlers-Danlos syndrome
1238:
Pierre Robin syndrome-faciodigital anomaly syndrome
920:Mandibuloacral dysplasia with type B lipodystrophy
583:Ehlers-Danlos syndrome, spondylodysplastic type, 1
136:, the following conditions feature micrognathism:
992:Microcephalic osteodysplastic primordial dwarfism
1964:
1091:Neonatal pseudo-hydrocephalic progeroid syndrome
933:Mandibulofacial dysostosis-microcephaly syndrome
1459:Thickened earlobes-conductive deafness syndrome
1205:Peroxisome biogenesis disorder 13A (Zellweger)
449:Congenital disorder of glycosylation, type IIw
446:Congenital disorder of glycosylation, type IIr
1799:
1214:Peroxisome biogenesis disorder 5A (Zellweger)
1211:Peroxisome biogenesis disorder 2A (Zellweger)
1208:Peroxisome biogenesis disorder 1A (Zellweger)
1009:Microcephaly 16, primary, autosomal recessive
976:Megalocornea-intellectual disability syndrome
1588:
1015:Microcephaly 4, primary, autosomal recessive
730:Micrognathism in Hutchinson-Gilford syndrome
580:Ehlers-Danlos syndrome, dermatosparaxis type
443:Congenital disorder of glycosylation type 1E
93:is undersized. It is also sometimes called
1806:
1792:
1561:
56:
1277:
1018:
725:
119:
111:
1330:Robinow syndrome, autosomal recessive 2
961:Mayer-Rokitansky-KĂĽster-Hauser syndrome
180:Acromegaloid facial appearance syndrome
14:
1965:
863:Lethal congenital contracture syndrome
439:Congenital contractural arachnodactyly
1787:
1640:"Micrognathia (Concept Id: C0025990)"
1428:-congenital disorder of glycosylation
1310:-congenital disorder of glycosylation
1220:-congenital disorder of glycosylation
914:Mandibuloacral dysplasia with type A
561:-congenital disorder of glycosylation
470:Congenital myopathy 22B, severe fetal
412:-congenital disorder of glycosylation
1314:Rhizomelic chondrodysplasia punctata
406:congenital disorder of glycosylation
400:congenital disorder of glycosylation
290:Autosomal recessive Robinow syndrome
251:Arthrogryposis multiplex congenita 5
226:Aprosencephaly cerebellar dysgenesis
205:congenital disorder of glycosylation
173:Acrofacial dysostosis Rodriguez type
116:Severe micrognathia in a 23-year-old
1282:Micrognathism in Carpenter syndrome
1185:Periventricular nodular heterotopia
1169:Otospondylomegaepiphyseal dysplasia
772:, autosomal dominant 64, 65, and 70
770:Intellectual developmental disorder
176:Acrofacial dysostosis, Catania type
27:Condition in which the jaw is small
24:
1100:Nestor-Guillermo progeria syndrome
363:Cerebrooculofacioskeletal syndrome
236:Arthrogryposis multiplex congenita
212:with pulmonary venous misalignment
25:
1984:
1661:
1355:Rubinstein-Taybi syndrome due to
1348:Rubinstein-Taybi syndrome due to
998:Microcephalic primordial dwarfism
937:Marbach-Rustad progeroid syndrome
782:Intellectual disability, X-linked
358:Cerebro-costo-mandibular syndrome
285:Autosomal recessive osteopetrosis
1952:Temporomandibular joint disorder
1444:X-linked intellectual disability
1409:Spondyloepimetaphyseal dysplasia
1180:Paris-Trousseau thrombocytopenia
1006:13, primary, autosomal recessive
467:Congenital myopathy 22A, classic
1112:, congenital hypomyelinating, 3
759:Infantile neuroaxonal dystrophy
343:Cardio-facio-cutaneous syndrome
254:Arthrogryposis, distal, type 2E
247:agenesis of the corpus callosum
1632:
1326:Roberts-SC phocomelia syndrome
1235:and rib and scapular anomalies
1196:Peroxisome biogenesis disorder
603:complementation groups L and P
534:4, with cardiovascular defects
504:, autosomal recessive, type 1B
459:Congenital myasthenic syndrome
455:, Saguenay-Lac-Saint-Jean type
421:Cold-induced sweating syndrome
13:
1:
1554:
1523:
714:Hereditary spastic paraplegia
141:11q partial monosomy syndrome
1610:10.1016/j.ijporl.2011.12.023
1511:
1382:Shprintzen-Goldberg syndrome
853:Lateral meningocele syndrome
518:Developmental and epileptic
508:D-2-hydroxyglutaric aciduria
231:Arterial tortuosity syndrome
210:Alveolar capillary dysplasia
158:4p partial monosomy syndrome
7:
1771:. Medline Plus. 12 May 2009
1532:
1163:Oto-palato-digital syndrome
1122:Oculodentodigital dysplasia
877:multiple pterygium syndrome
736:Hutchinson-Gilford syndrome
700:Hallermann-Streiff syndrome
280:multiple pterygium syndrome
146:3-methylglutaconic aciduria
10:
1989:
1491:Wiedemann-Steiner syndrome
1393:Smith-Lemli-Opitz syndrome
1320:Ritscher-Schinzel syndrome
1257:Pontocerebellar hypoplasia
1175:Pallister-Killian syndrome
1139:Orofacial-digital syndrome
924:Mandibulofacial dysostosis
542:protein-losing enteropathy
491:Cranioectodermal dysplasia
474:Cornelia de Lange syndrome
453:Congenital lactic acidosis
126:Pitt-Rogers-Danks Syndrome
29:
1914:
1877:
1856:
1825:
1739:
1669:
1469:Treacher Collins syndrome
1340:Rubinstein-Taybi syndrome
1334:Rothmund-Thomson syndrome
763:Infantile-onset X-linked
655:1, 2 (X-linked), 3, and 7
216:Amish lethal microcephaly
107:
89:is a condition where the
72:
64:
55:
47:
42:
1921:Jaw and base of cranium
1365:Schwartz-Jampel syndrome
1224:Phelan-McDermid syndrome
1145:Orofaciodigital syndrome
1000:due to ZNF335 deficiency
981:Melnick-Needles syndrome
909:Mandibuloacral dysplasia
827:Keppen-Lubinsky syndrome
387:Cleidocranial dysostosis
317:Bartsocas-Papas syndrome
258:Autism spectrum disorder
67:Wolf–Hirschhorn syndrome
30:Not to be confused with
1485:Whistling face syndrome
1464:Toriello-Carey syndrome
1398:Spinal muscular atrophy
1387:Silver-Russell syndrome
1263:Potocki-Lupski syndrome
1153:types 3, 10, 12, and 18
1151:Osteogenesis imperfecta
986:Menke-Hennekam syndrome
972:Meckel syndrome, type 1
838:Langer-Giedion syndrome
776:Intellectual disability
765:spinal muscular atrophy
670:Genitopatellar syndrome
653:Galloway-Mowat syndrome
642:Frank-Ter Haar syndrome
630:Fibromuscular dysplasia
526:Diamond-Blackfan anemia
497:Craniofacial microsomia
427:Cole-Carpenter syndrome
221:Andersen Tawil syndrome
1302:Restrictive dermopathy
1283:
1159:with cranial sclerosis
1024:
941:Marden-Walker syndrome
903:Lymphatic malformation
778:, autosomal dominant 1
741:Hydrolethalus syndrome
731:
607:Faundes-Banka syndrome
575:Ehlers-Danlos syndrome
464:Congenital myopathy 20
379:Chondrodysplasia with
328:Bowen-Conradi syndrome
323:Bohring-Opitz syndrome
307:Baller-Gerold syndrome
129:
117:
1281:
1229:Pierre Robin sequence
1171:, autosomal recessive
1124:, autosomal recessive
1066:Myofibrillar myopathy
1054:Mucopolysaccharidosis
1022:
956:Matthew-Wood syndrome
886:cerebellar hypoplasia
811:Pierre-Robin syndrome
729:
695:Hajdu-Cheney syndrome
553:Distal arthrogryposis
434:osteochondrodysplasia
392:Coffin-Siris syndrome
353:Catel-Manzke syndrome
338:Camptomelic dysplasia
185:Adams-Oliver syndrome
168:Acrofacial dysostosis
123:
115:
1869:Maxillary hypoplasia
1501:Yunis-Varon syndrome
1453:Tetraamelia syndrome
1268:Prolidase deficiency
897:Loeys-Dietz syndrome
799:Isolated congenital
532:Diaphragmatic hernia
293:Autosomal recessive
238:1, neurogenic, with
1297:Renpenning syndrome
1259:types 2E, 7, and 12
1157:Osteopathia striata
1104:Neu-Laxova syndrome
893:, severe congenital
690:Greenberg dysplasia
624:Fibrochondrogenesis
596:dysmorphic features
522:64, 77, 80, and 100
312:Barber-Say syndrome
302:congenital myopathy
277:Autosomal recessive
1901:Torus mandibularis
1740:External resources
1476:and arthrogryposis
1360:haploinsufficiency
1292:Carpenter syndrome
1284:
1095:Nephrotic syndrome
1081:skeletal dysplasia
1025:
911:progeroid syndrome
732:
637:progeroid syndrome
381:joint dislocations
369:CHARGE association
295:spastic paraplegia
268:Autosomal dominant
152:46,XY sex reversal
130:
118:
1960:
1959:
1896:Congenital epulis
1763:
1762:
1446:Claes-Jensen type
1432:Stickler syndrome
1420:Squalene synthase
1373:1, 2, 5, 8, and 9
1086:Nemaline myopathy
951:Marshall syndrome
832:Knobloch syndrome
720:Holoprosencephaly
612:Feingold syndrome
577:, classic-like, 2
570:Dysosteosclerosis
565:Dubowitz syndrome
548:DiGeorge syndrome
480:Costello syndrome
132:According to the
84:
83:
37:Medical condition
16:(Redirected from
1980:
1808:
1801:
1794:
1785:
1784:
1780:
1778:
1776:
1667:
1666:
1655:
1654:
1652:
1650:
1636:
1630:
1629:
1592:
1586:
1585:
1565:
1487:, recessive form
1474:Ventriculomegaly
1438:Stromme syndrome
1233:pectus excavatum
1191:Perlman syndrome
1079:-related lethal
845:-like syndrome,
747:Immunodeficiency
680:Granulocytopenia
666:perinatal lethal
587:Emanuel syndrome
555:types 2B1 and 5D
374:Chondrodysplasia
348:Cat eye syndrome
271:Robinow syndrome
124:Micrognathia in
79:Medical genetics
60:
40:
39:
21:
1988:
1987:
1983:
1982:
1981:
1979:
1978:
1977:
1963:
1962:
1961:
1956:
1910:
1906:Torus palatinus
1873:
1852:
1833:Jaw abnormality
1821:
1812:
1774:
1772:
1767:
1764:
1759:
1758:
1735:
1734:
1678:
1664:
1659:
1658:
1648:
1646:
1638:
1637:
1633:
1593:
1589:
1566:
1562:
1557:
1535:
1526:
1514:
1371:Seckel syndrome
1342:due to 16p13.3
1273:Pyknodysostosis
1133:Orofacial cleft
1116:Noonan syndrome
1038:Miller syndrome
967:Meckel syndrome
946:Marfan syndrome
858:Legius syndrome
822:Kabuki syndrome
675:Gordon syndrome
664:Gaucher disease
647:Fraser syndrome
514:Desmosterolosis
485:Cowden syndrome
432:Complex lethal
376:Blomstrand type
170:Cincinnati type
163:Achard syndrome
110:
38:
35:
28:
23:
22:
15:
12:
11:
5:
1986:
1976:
1975:
1958:
1957:
1955:
1954:
1949:
1948:
1947:
1942:
1934:
1933:
1932:
1927:
1918:
1916:
1912:
1911:
1909:
1908:
1903:
1898:
1893:
1887:
1885:
1875:
1874:
1872:
1871:
1866:
1860:
1858:
1854:
1853:
1851:
1850:
1845:
1840:
1835:
1829:
1827:
1823:
1822:
1817:involving the
1815:Dental disease
1811:
1810:
1803:
1796:
1788:
1782:
1781:
1769:"Micrognathia"
1761:
1760:
1757:
1756:
1744:
1743:
1741:
1737:
1736:
1733:
1732:
1721:
1710:
1695:
1679:
1674:
1673:
1671:
1670:Classification
1663:
1662:External links
1660:
1657:
1656:
1631:
1604:(3): 414–418.
1587:
1559:
1558:
1556:
1553:
1552:
1551:
1546:
1541:
1539:Human mandible
1534:
1531:
1525:
1522:
1513:
1510:
1509:
1508:
1503:
1498:
1493:
1488:
1482:
1477:
1471:
1466:
1461:
1456:
1450:
1447:
1440:
1435:
1429:
1423:
1417:
1412:
1406:
1401:
1395:
1390:
1384:
1379:
1377:SHORT syndrome
1374:
1368:
1362:
1353:
1346:
1337:
1331:
1328:
1323:
1317:
1311:
1305:
1299:
1294:
1276:
1275:
1270:
1265:
1260:
1254:
1251:Polymicrogyria
1248:
1239:
1236:
1226:
1221:
1215:
1212:
1209:
1206:
1203:
1193:
1188:
1182:
1177:
1172:
1166:
1160:
1154:
1148:
1147:types 6 and 14
1142:
1136:
1130:
1128:Ogden syndrome
1125:
1119:
1113:
1107:
1101:
1098:
1092:
1089:
1083:
1074:
1072:Nager syndrome
1069:
1063:
1057:
1051:
1045:
1040:
1035:
1034:, syndromic 12
1032:Microphthalmia
1029:
1017:
1016:
1013:
1010:
1007:
1001:
995:
989:
983:
978:
973:
970:
964:
958:
953:
948:
943:
938:
935:
930:
921:
918:
912:
906:
900:
894:
888:
879:
873:
872:-like syndrome
866:
865:1, 2, 7, and 9
860:
855:
850:
840:
835:
829:
824:
819:
818:-like syndrome
813:
807:
797:
791:
788:
785:
779:
773:
767:
761:
756:
750:
744:
738:
724:
723:
717:
711:
702:
697:
692:
687:
684:immunoglobulin
677:
672:
667:
661:
656:
650:
644:
639:
633:
627:
621:
615:
609:
604:
601:Fanconi anemia
598:
589:
584:
581:
578:
572:
567:
562:
556:
550:
545:
535:
529:
523:
520:encephalopathy
516:
511:
505:
499:
494:
488:
482:
477:
471:
468:
465:
462:
456:
450:
447:
444:
441:
436:
430:
424:
418:
416:Cohen syndrome
413:
407:
401:
395:
389:
384:
377:
371:
366:
360:
355:
350:
345:
340:
335:
330:
325:
320:
314:
309:
304:
298:
291:
288:
282:
274:
265:
255:
252:
249:
243:
233:
228:
223:
218:
213:
207:
198:
188:
182:
177:
174:
171:
165:
160:
155:
149:
143:
109:
106:
82:
81:
76:
70:
69:
62:
61:
53:
52:
49:
45:
44:
36:
26:
9:
6:
4:
3:
2:
1985:
1974:
1973:Jaw disorders
1971:
1970:
1968:
1953:
1950:
1946:
1943:
1941:
1938:
1937:
1935:
1931:
1930:Retrognathism
1928:
1926:
1923:
1922:
1920:
1919:
1917:
1913:
1907:
1904:
1902:
1899:
1897:
1894:
1892:
1889:
1888:
1886:
1884:
1880:
1876:
1870:
1867:
1865:
1864:Micrognathism
1862:
1861:
1859:
1855:
1849:
1846:
1844:
1841:
1839:
1836:
1834:
1831:
1830:
1828:
1824:
1820:
1816:
1809:
1804:
1802:
1797:
1795:
1790:
1789:
1786:
1770:
1766:
1765:
1755:
1751:
1750:
1746:
1745:
1742:
1738:
1731:
1727:
1726:
1722:
1720:
1716:
1715:
1711:
1709:
1705:
1704:
1700:
1696:
1694:
1690:
1689:
1685:
1681:
1680:
1677:
1672:
1668:
1645:
1641:
1635:
1627:
1623:
1619:
1615:
1611:
1607:
1603:
1599:
1591:
1583:
1579:
1575:
1571:
1564:
1560:
1550:
1549:Retrognathism
1547:
1545:
1544:Macrognathism
1542:
1540:
1537:
1536:
1530:
1521:
1519:
1518:X-Ray testing
1507:
1506:Zaki syndrome
1504:
1502:
1499:
1497:
1494:
1492:
1489:
1486:
1483:
1481:
1480:Vici syndrome
1478:
1475:
1472:
1470:
1467:
1465:
1462:
1460:
1457:
1454:
1451:
1448:
1445:
1441:
1439:
1436:
1434:types 1 and 2
1433:
1430:
1427:
1424:
1421:
1418:
1416:
1413:
1410:
1407:
1405:
1402:
1399:
1396:
1394:
1391:
1388:
1385:
1383:
1380:
1378:
1375:
1372:
1369:
1366:
1363:
1361:
1358:
1354:
1351:
1347:
1345:
1344:microdeletion
1341:
1338:
1335:
1332:
1329:
1327:
1324:
1321:
1318:
1316:types 1 and 2
1315:
1312:
1309:
1306:
1303:
1300:
1298:
1295:
1293:
1289:
1286:
1285:
1280:
1274:
1271:
1269:
1266:
1264:
1261:
1258:
1255:
1252:
1249:
1247:
1243:
1240:
1237:
1234:
1230:
1227:
1225:
1222:
1219:
1216:
1213:
1210:
1207:
1204:
1201:
1197:
1194:
1192:
1189:
1186:
1183:
1181:
1178:
1176:
1173:
1170:
1167:
1164:
1161:
1158:
1155:
1152:
1149:
1146:
1143:
1140:
1137:
1134:
1131:
1129:
1126:
1123:
1120:
1117:
1114:
1111:
1108:
1105:
1102:
1099:
1096:
1093:
1090:
1087:
1084:
1082:
1078:
1075:
1073:
1070:
1067:
1064:
1061:
1058:
1055:
1052:
1049:
1048:Mucolipidosis
1046:
1044:
1043:Mohr syndrome
1041:
1039:
1036:
1033:
1030:
1027:
1026:
1021:
1014:
1011:
1008:
1005:
1002:
999:
996:
993:
990:
987:
984:
982:
979:
977:
974:
971:
968:
965:
962:
959:
957:
954:
952:
949:
947:
944:
942:
939:
936:
934:
931:
929:
925:
922:
919:
917:
916:lipodystrophy
913:
910:
907:
904:
901:
898:
895:
892:
891:Liver disease
889:
887:
883:
882:Lissencephaly
880:
878:
874:
871:
867:
864:
861:
859:
856:
854:
851:
848:
844:
841:
839:
836:
833:
830:
828:
825:
823:
820:
817:
814:
812:
808:
806:
802:
798:
796:
792:
789:
786:
783:
780:
777:
774:
771:
768:
766:
762:
760:
757:
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748:
745:
742:
739:
737:
734:
733:
728:
721:
718:
715:
712:
710:
706:
703:
701:
698:
696:
693:
691:
688:
685:
681:
678:
676:
673:
671:
668:
665:
662:
660:
659:GAPO syndrome
657:
654:
651:
648:
645:
643:
640:
638:
634:
631:
628:
625:
622:
619:
616:
613:
610:
608:
605:
602:
599:
597:
593:
590:
588:
585:
582:
579:
576:
573:
571:
568:
566:
563:
560:
557:
554:
551:
549:
546:
543:
539:
536:
533:
530:
527:
524:
521:
517:
515:
512:
509:
506:
503:
500:
498:
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492:
489:
486:
483:
481:
478:
475:
472:
469:
466:
463:
460:
457:
454:
451:
448:
445:
442:
440:
437:
435:
431:
428:
425:
422:
419:
417:
414:
411:
408:
405:
402:
399:
396:
393:
390:
388:
385:
382:
378:
375:
372:
370:
367:
364:
361:
359:
356:
354:
351:
349:
346:
344:
341:
339:
336:
334:
331:
329:
326:
324:
321:
318:
315:
313:
310:
308:
305:
303:
300:Bailey-Bloch
299:
296:
292:
289:
286:
283:
281:
278:
275:
272:
269:
266:
263:
259:
256:
253:
250:
248:
244:
241:
237:
234:
232:
229:
227:
224:
222:
219:
217:
214:
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206:
202:
199:
196:
192:
189:
186:
183:
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178:
175:
172:
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166:
164:
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159:
156:
153:
150:
147:
144:
142:
139:
138:
137:
135:
127:
122:
114:
105:
103:
99:
97:
92:
88:
87:Micrognathism
80:
77:
75:
71:
68:
63:
59:
54:
50:
46:
43:Micrognathism
41:
33:
32:Retrognathism
19:
1936:Dental arch
1863:
1843:Orthodontics
1838:malocclusion
1773:. Retrieved
1747:
1723:
1712:
1697:
1682:
1647:. Retrieved
1643:
1634:
1601:
1597:
1590:
1576:(4): 231–4.
1573:
1569:
1563:
1527:
1515:
1242:Poikiloderma
1118:1, 2, and 13
1004:Microcephaly
816:Isotretinoin
795:cleft palate
722:13, X-linked
709:hypothalamus
632:, multifocal
383:, gPAPP type
131:
94:
86:
85:
18:Micrognathia
1925:Prognathism
1749:MedlinePlus
1246:neutropenia
1056:, MPS-I-H/S
801:hypoglossia
686:abnormality
618:FG syndrome
476:1, 3, and 5
148:, type VIIB
48:Other names
1725:DiseasesDB
1555:References
1524:Treatments
1442:Syndromic
1422:deficiency
1110:Neuropathy
502:Cutis laxa
333:C syndrome
264:deficiency
195:otocephaly
102:intubation
98:hypoplasia
96:mandibular
65:Girl with
1940:Crossbite
1891:Cherubism
1848:Gnathitis
1618:0165-5876
1512:Diagnosis
1352:mutations
1290:-related
1200:Zellweger
1165:, type II
1097:, type 11
969:13 and 14
809:Isolated
793:Isolated
705:Hamartoma
635:Fontaine
74:Specialty
1967:Category
1945:Overbite
1883:Mandible
1649:April 2,
1626:22245167
1533:See also
994:, type 3
928:alopecia
805:aglossia
592:Epilepsy
538:Diarrhea
394:6 and 12
191:Agnathia
1879:Maxilla
1826:General
1719:D008844
1582:7883869
1455:1 and 2
1389:1 and 2
1322:1 and 3
1106:1 and 2
1062:1 and 2
1050:type II
988:1 and 2
899:1 and 2
884:7 with
875:Lethal
868:Lethal
743:1 and 2
493:2 and 3
487:5 and 6
319:1 and 2
297:type 70
260:due to
197:complex
1775:21 May
1754:003306
1708:524.04
1624:
1616:
1580:
1367:type 1
1350:CREBBP
1336:type 2
963:type 2
870:Kniest
847:B3GAT3
843:Larsen
614:type 1
559:DPAGT1
242:defect
240:myelin
128:(PRDS)
108:Causes
1915:Other
1730:22641
1693:K07.0
1357:EP300
1288:RAB23
1244:with
1231:with
1198:10A (
926:with
682:with
262:AUTS2
1881:and
1857:Size
1777:2011
1714:MeSH
1703:9-CM
1651:2024
1644:NCBI
1622:PMID
1614:ISSN
1578:PMID
1426:SSR4
1308:RFT1
1218:PGM1
1077:NEK9
849:type
544:type
540:10,
410:COG8
404:COG7
398:COG1
201:ALG1
134:NCBI
1819:jaw
1699:ICD
1684:ICD
1606:doi
707:of
365:1-4
273:1-3
91:jaw
1969::
1752::
1728::
1717::
1706::
1691::
1688:10
1642:.
1620:.
1612:.
1602:76
1600:.
1574:14
1572:.
1520:.
1141:IV
1135:13
784:61
749:49
716:23
461:19
1807:e
1800:t
1793:v
1779:.
1701:-
1686:-
1676:D
1653:.
1628:.
1608::
1584:.
1304:1
1202:)
1187:7
1088:9
1068:8
905:6
834:2
803:/
755:1
649:3
626:2
620:1
510:1
429:1
423:1
287:5
203:-
193:-
187:2
154:4
34:.
20:)
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