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The cerebro-costo-mandibular syndrome: 9-year follow-up of a case, 12/2000
Cerebro-costo-mandibular syndrome (CCMS) is a rare multiple congenital anomaly with a low survival rate. There are few reports of long-term survival in this... 
Cerebro- costo- mandibular syndrome, micrognathia, posterior rib gap defects
Journal
Ear, Nose and Throat Journal, ISSN 0145-5613, 2019, p. 14556131985564
Journal Article
Toxicology Letters, ISSN 0378-4274, 02/2020, Volume 319, pp. 250 - 255
The effect of thalidomide on mandibular development is unclear. In this study, thalidomide was delivered to pregnant rabbits from the 8th to 14th day of... 
Micrognathia | Drug | Craniofacial development | Animal model | Vegf-α | Hematoma
Journal Article
American Journal of Medical Genetics. Part A, ISSN 1552-4825, 06/2018, Volume 176, Issue 6, p. 1349
The triad of micrognathia, glossoptosis, and concomitant airway obstruction defined as "Robin sequence" (RS) is caused by oropharyngeal developmental events... 
genetics | micrognathia | cleft palate | Robinsequence | embryology | glossoptosis | Pierre Robin sequence
Journal Article
CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY, ISSN 0390-6663, 2019, Volume 46, Issue 1, pp. 131 - 135
Femoral hypoplasia-unusual facies syndrome (FH-UFS), also known as femoral-facial syndrome, is an extremely rare condition. The diagnostic criteria for this... 
Micrognathia | Femoral agenesis | Diabetes mellitus | AGENESIS | PREGNANCY | OBSTETRICS & GYNECOLOGY
Journal Article
Clinics in Perinatology, ISSN 0095-5108, 12/2018, Volume 45, Issue 4, pp. 609 - 628
Journal Article
BMC Anesthesiology, 11/2019, Volume 19, Issue 1, pp. 1 - 8
Abstract Background Airway management is challenging in children with Robin sequence (RS) requiring mandibular distraction osteogenesis (MDO). We derived and... 
Mandibular micrognathia | Robin sequence | Difficult intubation
Journal Article
by Jia, W and He, Y and Helal, H and Wang, Y and Li, J
British Journal of Oral & Maxillofacial Surgery, ISSN 0266-4356, 09/2019, Volume 57, Issue 7, pp. 701 - 703
Journal Article
Sleep Medicine, ISSN 1389-9457, 03/2018, Volume 43, pp. 96 - 99
To evaluate the association of polysomnographic parameters with clinical symptom severity in Robin sequence (RS) patients. All patients diagnosed as presenting... 
Micrognathia | Pierre Robin syndrome | Glossoptosis | Polysomnography | Respiratory sounds | Laryngoscopy | DISTRACTION | INFANTS | SLEEP-APNEA | CLINICAL NEUROLOGY | CHILDREN | Oxyhemoglobin
Journal Article
ACTA MEDICA OKAYAMA, ISSN 0386-300X, 2019, Volume 73, Issue 3, pp. 273 - 277
Nager syndrome is a rare disease involving severe micrognathia and upper limb shortening. In this report, we describe a case in which micrognathia of the fetus... 
SF3B4 | MEDICINE, RESEARCH & EXPERIMENTAL | jaw index | acrofacial dysostosis | MANAGEMENT | Nager syndrome | micrognathia | HAPLOINSUFFICIENCY
Journal Article
Journal of Oral and Maxillofacial Surgery, ISSN 0278-2391, 05/2018, Volume 76, Issue 5, pp. 1058 - 1064
The etiology of the palatal cleft in Robin sequence (RS) is unknown. The purpose of this study was to assess the position of the fetal tongue at prenatal... 
MICE | SOX9 | MICROGNATHIA | DENTISTRY, ORAL SURGERY & MEDICINE | DEFECT | Medicine, Experimental | Medical research | Cleft palate | Magnetic resonance imaging | Pregnant women
Journal Article
08/2012
We present a case with a 4p terminal deletion, evidenced in GTG-banded chromosome study. Phenotypic signs described in the classical Wolf-Hirschhorn syndrome... 
micrognathia | karyotyping | Chromosomes | chromosome deletion | Wolf-Hirschhorn syndrome
Web Resource
Indian Pediatrics, ISSN 0019-6061, 08/2013, Volume 50, Issue 8, pp. 795 - 796
3p deletion is a rare cytogenetic finding. Here we describe a 3 months old male with congenital malformations. His karyotype revealed 3p deletion... 
trignocephaly | micrognathia | 3p deletion | PEDIATRICS | PATIENT | FEATURES
Journal Article
Paediatrics and Child Health, ISSN 1751-7222, 11/2019
Journal Article
Annals of Plastic Surgery, ISSN 0148-7043, 04/2019, Volume 82, Issue 4S Suppl 3, pp. S242 - S246
BACKGROUNDPrenatal ultrasound is the standard modality to screen for fetal craniofacial malformations, but can be limited by sonographer experience,... 
SURGERY | MRI | craniofacial | cleft palate | congenital | anomalies | orofacial cleft | fetal MRI | cleft lip | LIP | ULTRASOUND | micrognathia | prenatal | INFANTS | prenatal diagnosis | Cleft palate | Prenatal diagnosis | Diagnosis | Magnetic resonance imaging | Comparative analysis | Methods
Journal Article
Ultrasound, ISSN 1742-271X, 5/2017, Volume 25, Issue 2, pp. 115 - 119
Pena–Shokeir phenotype is a lethal anomaly characterized by neurogenic arthrogryposis, craniofacial anomalies, and pulmonary hypoplasia. This syndrome should... 
Pena–Shokeir phenotype | Arthrogryposis | hyperlordosis | micrognathia | Case Reports
Journal Article
Plastic and Reconstructive Surgery, ISSN 0032-1052, 03/2014, Volume 133, Issue 3, pp. 352e - 359e
Journal Article
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