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Fetal micrognathia

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https://www.readbyqxmd.com/read/30328631/objective-assessment-of-the-fetal-facial-profile-at-second-and-third-trimester-of-pregnancy
#1
Jing Lu, Daljit Singh Sahota, Liona C Poon, Yuen Ha Ting, Yvonne Kwun Yue Cheng, Yue Wang, Tak Yeung Leung
OBJECTIVE: To investigate the intra- and inter-observer reproducibility of a novel sonographic parameter named facial maxillary angle (FMA), and to establish nomograms of FMA, inferior facial angle (IFA), frontal nasal-mental angle (FNMA), maxilla-nasion-mandible angle (MNMA) and fetal profile line (FPL) in Chinese fetuses. METHODS: In this prospective cross-sectional study, FMA, IFA, FNMA, MNMA and FPL were measured in 592 normal fetuses between 16 and 36 gestational weeks...
October 17, 2018: Prenatal Diagnosis
https://www.readbyqxmd.com/read/29554458/in-utero-glossoptosis-in-fetuses-with-robin-sequence-measurements-from-prenatal-mri
#2
Cory M Resnick, Tessa D Kooiman, Carly E Calabrese, Ryne Didier, Bonnie L Padwa, Judy A Estroff, Maarten J Koudstaal
OBJECTIVE: Glossoptosis causes airway obstruction in patients with Robin sequence (RS), but little is known about the in-utero tongue. The purpose of this study was to assess shape and position of the fetal tongue on prenatal magnetic resonance imaging (MRI) to determine if this is predictive of postnatal RS. DESIGN: Retrospective case-control study including fetuses with prenatal MRIs performed from 2002 to 2017. Inclusion criteria were (1) prenatal MRI of adequate quality, (2) live born and evaluated postnatally for craniofacial findings...
April 2018: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/29460382/an-algorithm-for-predicting-robin-sequence-from-fetal-mri
#3
Cory M Resnick, Tessa D Kooiman, Carly E Calabrese, David Zurakowski, Bonnie L Padwa, Maarten J Koudstaal, Judy A Estroff
BACKGROUND: Infants with Robin sequence (RS) may present with airway compromise at delivery. Prenatal diagnosis would improve preparation and postnatal care. The purpose of this study was to devise a predictive algorithm for RS based on fetal magnetic resonance imaging (MRI). METHODS: Retrospective case-control study including fetal MRIs from 2002 to 2017. Inclusion criteria were (1) MRI of adequate quality, (2) live-born infant, and (3) postnatal evaluation. Subjects were grouped on the basis of postnatal diagnosis: (1) RS (micrognathia, glossoptosis, airway obstruction), (2) micrognathia without airway obstruction ("micrognathia"), (3) cleft lip and palate ("CLP"), and (4) gestational age-matched controls...
April 2018: Prenatal Diagnosis
https://www.readbyqxmd.com/read/29396778/fetal-valproate-syndrome-the-irish-experience
#4
Hamizah Mohd Yunos, Andrew Green
INTRODUCTION: Fetal valproate syndrome was first described in 1984. Valproic acid crosses the placenta and can potentially lead to major congenital malformation, dysmorphism and neurodevelopmental disorder. METHODS: A retrospective study of 29 cases of FVS diagnosed by geneticists from 1995 to 2016. The cases were diagnosed based on criteria of fetal anticonvulsant syndrome. RESULTS: A total of 29 cases reported in the last 21 years. Features commonly described are prominent metopic ridge, midface hypoplasia, epicanthic folds, micrognathia and broad and flat nasal bridge...
February 3, 2018: Irish Journal of Medical Science
https://www.readbyqxmd.com/read/28567106/antenatal-ultrasonography-findings-and-magnetic-resonance-imaging-in-a-case-of-pena-shokeir-phenotype
#5
Xuan-Hong Tomai, Thanh-Xuan Jasmine, Thanh-Hai Phan
Pena-Shokeir phenotype is a lethal anomaly characterized by neurogenic arthrogryposis, craniofacial anomalies, and pulmonary hypoplasia. This syndrome should be distinguished from trisomy 18 and arthrogryposis multiplex congenita for better counseling and establishing fetal prognosis. We present the case of a pregnant woman diagnosed with a Pena-Shokeir phenotype affected fetus at 24 weeks of gestation. Prenatal ultrasonography and fetal magnetic resonance imaging detected persistent hyperextension of the lumbar spine, micrognathia, absent septum pellucidum, and all characteristic features of Pena-Shokeir phenotype...
May 2017: Ultrasound: Journal of the British Medical Ultrasound Society
https://www.readbyqxmd.com/read/28489513/thyroid-function-during-early-life-and-dental-development
#6
S Vucic, T I M Korevaar, B Dhamo, V W V Jaddoe, R P Peeters, E B Wolvius, E M Ongkosuwito
Children with low levels of thyroid hormones (hypothyroidism) have delayed tooth eruption, enamel hypoplasia, micrognathia, and anterior open bite, whereas children with hyperthyroidism may suffer from accelerated tooth eruption, maxillary, and mandibular osteoporosis. However, it is still unknown whether thyroid function variations within the normal or subclinical range also have an impact on hard dental tissues in healthy children. The objective of this study was, therefore, to investigate the association between thyroid function from the fetal period until early childhood and dental development at school age...
August 2017: Journal of Dental Research
https://www.readbyqxmd.com/read/28070244/assessment-of-fetus-during-second-trimester-ultrasonography-using-hdlive-software-what-is-its-real-application-in-the-obstetrics-clinical-practice
#7
Gabriele Tonni, Gianpaolo Grisolia, Eduardo Félix Santana, Edward Araujo Júnior
AIM: To show imaging results from application of four-dimensional (4D) ultrasound lightening technique (HDlive™) in clinical obstetrics practice. METHODS: Normal and abnormal fetuses at second and third trimester of pregnancy undergoing routine scan with 4D HDlive™ (5DUS) in the rendering mode are described. Realistic features of fetal structures were provided by 5DUS in the rendering mode. Normal anatomy as well as pathology like cleft lip, hypoplastic face, micrognathia, low-set ears, corpus callosum, arthrogryposis, aortic arch, left congenital diaphragmatic hernia are highlighted in this study...
December 28, 2016: World Journal of Radiology
https://www.readbyqxmd.com/read/27751653/recurrent-de-novo-bicd2-mutation-associated-with-arthrogryposis-multiplex-congenita-and-bilateral-perisylvian-polymicrogyria
#8
Gianina Ravenscroft, Nataliya Di Donato, Gabriele Hahn, Mark R Davis, Paul D Craven, Gemma Poke, Katherine R Neas, Teresa M Neuhann, William B Dobyns, Nigel G Laing
Autosomal dominantly inherited mutations of BICD2 are associated with congenital-onset spinal muscular atrophy characterised by lower limb predominance. A few cases have also showed upper motor neuron pathology, including presenting with features resembling hereditary spastic paraplegia. The age-of-onset for the published families is usually at birth but also included cases with childhood- and adult-onset disease. In this report we described two isolated probands that presented in utero with features associated with reduced fetal movements...
November 2016: Neuromuscular Disorders: NMD
https://www.readbyqxmd.com/read/27329096/goldenhar-syndrome-a-rare-diagnosis-with-possible-prenatal-findings
#9
Bárbara Ribeiro, Joana Igreja, Miguel Gonçalves-Rocha, Alexandra Cadilhe
Goldenhar syndrome is a rare congenital disease associated with hemifacial hypoplasia as well as ear and ocular defects. Sometimes it is also associated with vertebral and other bone defects, cardiac malformations and central nervous system anomalies. Its aetiology is not yet clarified in the literature. We present a case of multiple malformations detected in the morphology ultrasound (at 22 weeks of gestation), namely absent nasal bones, micrognathia and absent left radius, among other defects. Genetic counselling, fetal brain MRI and cardiac sonography, which showed ventricular septal defect, were performed...
June 21, 2016: BMJ Case Reports
https://www.readbyqxmd.com/read/27312123/prenatal-features-of-pena-shokeir-sequence-with-atypical-response-to-acoustic-stimulation
#10
Sirida Pittyanont, Phudit Jatavan, Songkiat Suwansirikul, Theera Tongsong
A fetal sonographic screening examination performed at 23 weeks showed polyhydramnios, micrognathia, fixed postures of all long bones, but no movement and no breathing. The fetus showed fetal heart rate acceleration but no movement when acoustic stimulation was applied with artificial larynx. All these findings persisted on serial examinations. The neonate was stillborn at 37 weeks and a final diagnosis of Pena-Shokeir sequence was made. In addition to typical sonographic features of Pena-Shokeir sequence, fetal heart rate accelerations with no movement in response to acoustic stimulation suggests that peripheral myopathy may possibly play an important role in the pathogenesis of the disease...
September 2016: Journal of Clinical Ultrasound: JCU
https://www.readbyqxmd.com/read/27306473/smith-lemli-opitz-syndrome-a-challenging-prenatal-diagnosis
#11
Agata Szpera-Goździewicz, Mariola Ropacka-Lesiak, Paweł Rzymski, Grzegorz H Bręborowicz
The aim of the study was to present a case of Smith-Lemli-Opitz syndrome (SLOS) in a fetus of a 33-year-old patient. At 31 weeks of gestation, the following fetal malformations were detected on an ultrasound: atrioventricular septal defect (AVSD), aortic coarctation, shortening of the lower limbs, narrow forehead, hyperthelorism, micrognathia, anteverted nares, ambiguous genitalia, and signs of intrauterine growth restriction. The baby died 11 days after birth. Further genetic screening of the parents revealed the 7-DHCR enzyme mutation in both of them...
2016: Ginekologia Polska
https://www.readbyqxmd.com/read/27278992/three-dimensional-sonographic-features-of-a-fetus-with-wolf-hirschhorn-syndrome
#12
Tharangrut Hanprasertpong, Uiko Hanaoka, Xia Zhang, Nobuhiro Mori, Eisuke Inubashiri, Kenji Kanenishi, Chizu Yamashiro, Hirokazu Tanaka, Atsuko Shiota, Toshihiro Yanagihara, Toshiyuki Hata
We present a case of fetal Wolf-Hirschhorn syndrome diagnosed by conventional two-dimensional and three-dimensional ultrasonography. Conventional two-dimensional ultrasonography revealed a diaphragmatic hernia, nuchal edema, and suspected hypospadias. Three-dimensional ultrasonography clearly showed a flattening of the face, a high forehead, a broad nasal bridge continuing to the forehead, exophthalmos, and micrognathia (resembling the appearance of a Greek warrior helmet), but conventional two-dimensional ultrasonography did not depict these findings...
December 2008: Journal of Medical Ultrasonics
https://www.readbyqxmd.com/read/27219269/prenatal-features-predictive-of-robin-sequence-identified-by-fetal-magnetic-resonance-imaging
#13
Carolyn R Rogers-Vizena, John B Mulliken, Kimberly M Daniels, Judy A Estroff
BACKGROUND: Prenatal magnetic resonance imaging is increasingly used to detect congenital anomalies. The purpose of this study was to determine whether prenatal magnetic resonance imaging accurately characterizes features predictive of postnatal Robin sequence so that possible airway compromise and feeding difficulty at birth can be anticipated. METHODS: The authors retrospectively identified pregnant women who underwent fetal magnetic resonance imaging between 2002 and 2014 and were found to be carrying a fetus with micrognathia...
June 2016: Plastic and Reconstructive Surgery
https://www.readbyqxmd.com/read/27185679/anesthetic-management-of-an-ex-utero-intrapartum-treatment-procedure-a-novel-balanced-approach
#14
Adam Braden, Christopher Maani, Christopher Nagy
Ex utero intrapartum treatment (EXIT) procedures are therapeutic interventions for fetuses with life-threatening airway abnormalities and/or other prenatally diagnosed congenital malformations requiring immediate neonatal extracorporeal membrane oxygenation support. Although certain anesthetic goals are common among EXIT procedures, many different approaches to their management have been described in the literature. Herein, we present a novel anesthetic approach to an EXIT procedure for fetal micrognathia and retrognathia...
June 2016: Journal of Clinical Anesthesia
https://www.readbyqxmd.com/read/26419098/-two-cases-of-fetuses-with-difficult-airway-that-survived-by-the-exit-ex-utero-intrapartum-treatment-procedure
#15
Tetsuya Kai, Natsuki Ishibe, Yuji Soeda, Mariko Tanaka, Sumio Hoka
We successfully managed two fetuses complicated with suspected airway obstruction after birth by the EXIT (ex utero intrapartum treatment) procedure, whose placental circulation was maintained till their airway was secured during the cesarean section. The first fetus was suspected to have airway obstruction due to a large neck mass. At 36 weeks of gestation, the EXIT procedure was undertaken performing the tracheal intubation successfully by laryngoscope. The second fetus with micrognathia was expected to have airway obstruction after birth...
April 2015: Masui. the Japanese Journal of Anesthesiology
https://www.readbyqxmd.com/read/26349195/a-variant-case-of-6p24-deletion-syndrome-omim-612582
#16
R N Ergin, E Cigerciogullari, Y Alanay, M Yayla
The 6p24 deletion syndrome, a contiguous gene deletion syndrome is characterized by a wide spectrum of clinical presentations. In this case report we present an antenatal case of 6p 24 deletion syndrome variant involving FOXC1 gene. First trimester fetal screening of a 34 year old pregnant female revealed ultrasonographic anomalies and chorionic villus sampling was performed to rule out any chromosomal anomaly. Cytogenetic examination resulted in normal 46,XY karyotype. In the following weeks further anomalies like cleft palate/lip, thick nuchal fold, ventral septal defect and low set ear were detected with ultrasonography...
2015: Genetic Counseling
https://www.readbyqxmd.com/read/26138114/registry-analysis-supports-different-mechanisms-for-gastroschisis-and-omphalocele-within-shared-developmental-fields
#17
Bonna Benjamin, Golder N Wilson
Nine thousand two hundred eighty abnormalities associated with 2,943 abdominal wall defects (AWD) encoded from 1999 to 2008 by the Texas Birth Defects Registry (TBDR) were classified and analyzed for mechanism, beginning with 1,831 gastroschisis cases, 774 (41%) with 2,368 associated anomalies (AA) and 814 of omphalocele, 727 (89%) with 4,092 AA. Typical AA profiles for Trisomy 18 (23% of omphalocele cases) and Beckwith-Wiedemann syndrome (15%) validated registry AA descriptors, chromosome disorders surprisingly accounting for 24% of known conditions with gastroschisis followed by expected amniotic band (ADAM) complex (23%) and amyoplasia/arthrogryposis (16%)...
November 2015: American Journal of Medical Genetics. Part A
https://www.readbyqxmd.com/read/25982360/prenatal-diagnosis-of-pierre-robin-sequence-accuracy-and-ability-to-predict-phenotype-and-functional-severity
#18
Katia Lind, Marie-Cécile Aubry, Nadia Belarbi, Christel Chalouhi, Gérard Couly, Alexandra Benachi, Stanislas Lyonnet, Véronique Abadie
OBJECTIVE: To assess the outcome of fetuses who had sonographic features suggestive of Pierre Robin Sequence (PRS). METHOD: All prenatal ultrasounds that mentioned 'posterior cleft palate', or 'micro or retrognathia' or 'PRS' over 13 and 20 years, respectively, at two obstetrical centers were reviewed. Medical records for children with isolated PRS monitored over 20 years at a PRS referral center for prenatal anomalies and the severity of neonatal feeding and respiratory functional disorders were utilized for comparison...
September 2015: Prenatal Diagnosis
https://www.readbyqxmd.com/read/25967128/prenatal-identification-of-pierre-robin-sequence-a-review-of-the-literature-and-look-towards-the-future
#19
REVIEW
Matthew G Kaufman, Christopher I Cassady, Charles H Hyman, Wesley Lee, Mehernoor F Watcha, Helena K Hippard, Olutoyin A Olutoye, David Y Khechoyan, Laura A Monson, Edward P Buchanan
Fetal ultrasonography is an important tool used to prenatally diagnose many craniofacial conditions. Pierre Robin sequence (PRS) is a rare congenital deformation characterized by micrognathia, glossoptosis, and airway obstruction. PRS can present as a perinatal emergency when the retropositioned tongue obstructs the airway leading to respiratory compromise. More predictable and reliable diagnostic studies could help the treating medical team as well as families prepare for these early airway emergencies. The medical literature was reviewed for different techniques used to prenatally diagnose PRS radiologically...
2016: Fetal Diagnosis and Therapy
https://www.readbyqxmd.com/read/25913727/identification-of-a-premature-stop-codon-mutation-in-the-phgdh-gene-in-severe-neu-laxova-syndrome-evidence-for-phenotypic-variability
#20
Eduardo P Mattos, André Anjos da Silva, José Antônio A Magalhães, Júlio César L Leite, Sandra Leistner-Segal, Rejane Gus-Kessler, Juliano Adams Perez, Leonardo M Vedolin, Albertina Torreblanca-Zanca, Pablo Lapunzina, Victor L Ruiz-Perez, Maria Teresa V Sanseverino
In some cases Neu-Laxova syndrome (NLS) is linked to serine deficiency due to mutations in the phosphoglycerate dehydrogenase (PHGDH) gene. We describe the prenatal and postnatal findings in a fetus with one of the most severe NLS phenotypes described so far, caused by a homozygous nonsense mutation of PHGDH. Serial ultrasound (US) and pre- and postnatal magnetic resonance imaging (MRI) evaluations were performed. Prenatally, serial US evaluations suggested symmetric growth restriction, microcephaly, hypoplasia of the cerebellar vermis, micrognathia, hydrops, shortened limbs, arthrogryposis, and talipes equinovarus...
June 2015: American Journal of Medical Genetics. Part A
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