Works matching DE "MICROGNATHIA"

Results: 284

Two Chinese Patients of Auriculocondylar Syndrome 2: A Novel PLCB4 Splicing Variant and 5-Year Follow-up.

Published in:

Cleft Palate Craniofacial Journal, 2025, v. 62, n. 6, p. 914, doi. 10.1177/10556656241234575

By:

Lin, Yunting;
Zhang, Ye;
Ma, Jian;
Liu, Shu;
Liu, Yongxi;
Yang, Chaoxiang;
Zeng, Chunhua;
Luo, Xianqiong

Publication type:

Article

Neonatal Functional Treatment for Pierre Robin Sequence.

Published in:

Turkish Journal of Orthodontics, 2019, v. 32, n. 3, p. 151, doi. 10.5152/TurkJOrthod.2019.18057

By:

Galluccio, Gabriella;
Mazzoli, Valentina;
Vernucci, Roberto;
Silvestri, Alessandro;
Barbato, Ersilia

Publication type:

Article

Clinical Characteristics of the Cleft Lip and/or Palate: Association with Congenital Anomalies, Syndromes, and Chromosomal Anomalies.

Published in:

Yonago Acta Medica, 2023, v. 66, n. 4, p. 440, doi. 10.33160/yam.2023.11.009

By:

Nobuyuki Fujii;
Rieko Doi;
Takashi Narai;
Naoki Chiuriki;
Mika Ikuta;
Isamu Kodani

Publication type:

Article

Recurrent Erythema Nodosum in a Child with a SHOC2 Gene Mutation.

Published in:

Yonago Acta Medica, 2019, v. 62, n. 1, p. 159, doi. 10.33160/yam.2019.03.022

By:

Tetsuya Okazaki;
Yoshiaki Saito;
Kazunari Sugita;
Kanae Nosaka;
Koyo Ohno;
Yumie Hiraoka;
Noriko Kasagi;
Mitsutaka Ebiki;
Satoshi Narai;
Yuki Kawashima;
Shuichi Takano;
Masachika Kai;
Kaori Adachi;
Osamu Yamamoto;
Eiji Nanba;
Yoshihiro Maegaki

Publication type:

Article

Anaesthesia recommendations for Congenital cataracts, facial dysmorphism and neuropathy syndrome.

Published in:

Anaesthesiologie & Intensivmedizin, 2023, v. 64, p. 1, doi. 10.19224/ai2023.S446

By:

Hudec, Jan;
Kosinová, Martina

Publication type:

Article

Mortality in Robin sequence: identification of risk factors.

Published in:

2018

By:

Logjes, Robrecht J. H.;
Haasnoot, Maartje;
Lemmers, Petra M. A.;
Nicolaije, Mike F. A.;
van den Boogaard, Marie-José H.;
van der Molen, Aebele B. Mink;
Breugem, Corstiaan C.;
Mink van der Molen, Aebele B

Publication type:

journal article

Assessment of dysphagia in infants with facial malformations.

Published in:

2009

By:

Baudon, Jean-Jacques;
Renault, Francis;
Goutet, Jean-Michel;
Biran-Mucignat, Valérie;
Morgant, Georges;
Garabedian, Erea-Noel;
Vazquez, Marie-Paule;
Biran-Mucignat, Valérie

Publication type:

journal article

Oculocutaneous albinism accompanied by minor morphologic stigmata.

Published in:

2008

By:

Castro-Gago, Manuel

Publication type:

commentary

Sizes of dental arches in young adult patients with Pierre Robin sequence and isolated cleft palate.

Published in:

Acta Odontologica Scandinavica, 1998, v. 56, n. 2, p. 85, doi. 10.1080/00016359850136030

By:

Laitinen, Sirpa H.;
Ranta, Reijo

Publication type:

Article

Triad of Micrognathia, Oligodontia, and Ankyloglossia in a Non-Syndromic Individual: A Case Report with Rare Presentation.

Published in:

2024

By:

Shukla, Priti;
Sharma, Varsha;
Acharya, Shivesh;
Singh, Shruti

Publication type:

Case Study

Edward's syndrome with a novel karyotype.

Published in:

Bangladesh Journal of Medical Science, 2011, v. 10, n. 3, p. 211, doi. 10.3329/bjms.v10i3.8368

By:

Patra, S.;
Garg, A.;
Gulati, A.;
Krishnamurthy, S.;
Aneja, S.

Publication type:

Article

Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 8, p. 1019, doi. 10.1038/ejhg.2008.90

By:

Hosoki, Kana;
Ogata, Tsutomu;
Kagami, Masayo;
Tanaka, Touju;
Saitoh, Shinji

Publication type:

Article

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 265, doi. 10.1038/sj.ejhg.5200950

By:

Melkoniemi, Miia;
Koillinen, Hannele;
Mannikko, Minna;
Warman, Matthew L;
Pihlajamaa, Tero;
Kaariainen, Helena;
Rautio, Jorma;
Hukki, Jyri;
Stofko, Joseph A;
Cisneros, George J;
Krakow, Deborah;
Cohn, Daniel H;
Kere, Juha;
Ala-Kokko, Leena

Publication type:

Article

Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15.

Published in:

Molecular Cytogenetics (17558166), 2017, v. 10, p. 1, doi. 10.1186/s13039-017-0339-z

By:

Tewari, Stuti;
Lubna, Naznin;
Shah, Raju;
Al-Rikabi, Ahmed B. H.;
Shah, Krati;
Sheth, Jayesh;
Sheth, Frenny

Publication type:

Article

Nadir bir seks kromozom bozukluğu: 48,XXYY sendromu.

Published in:

Türk Pediatri Arşivi, 2016, v. 51, n. 2, p. 106, doi. 10.5152/TurkPediatriArs.2016.1551

By:

Atik, Tahir;
Çoğulu, Özgür;
Özkınay, Ferda

Publication type:

Article

Micrognathia and cleft palate as a cause of obstructive sleep apnoea in infants.

Published in:

Acta Paediatrica, 2025, v. 114, n. 6, p. 1169, doi. 10.1111/apa.17540

By:

Kirjavainen, Turkka;
Vuola, Pia;
Suominen, Janne;
Saarikko, Anne

Publication type:

Article

Neonatal outcomes of foetal micrognathia: An 11‐year review.

Published in:

Acta Paediatrica, 2022, v. 111, n. 12, p. 2284, doi. 10.1111/apa.16537

By:

Sammut, Audrienne;
Knight, Caroline L.;
O'Sullivan, Hannah Rosen;
Meau‐Petit, Virginie

Publication type:

Article

A case with oto-spondylo-mega-epiphyseal-dysplasia (OSMED): the clinical recognition and differential diagnosis.

Published in:

Turkish Journal of Pediatrics, 2011, v. 53, n. 3, p. 346

By:

Karaer, Kadri;
Rosti, Rasim Özgür;
Torun, Deniz;
Sanal, Hatice Tuba;
Bahçe, Muhterem;
Güran, Şefik

Publication type:

Article

Airway management in neonates with Pierre Robin sequence.

Published in:

Turkish Journal of Pediatrics, 2010, v. 52, n. 2, p. 167

By:

Gözü, Aydın;
Genç, Bülent;
Palabıyık, Murat;
Unal, Murat;
Yıldırım, Güven;
Kavuncuoğlu, Sultan;
Özsoy, Zafer

Publication type:

Article

A report of a patient with duplication of 7p13→pter and deletion of 2p23→pter due to a maternal 2p;7p translocation.

Published in:

Turkish Journal of Pediatrics, 2009, v. 51, n. 2, p. 174

By:

Türköver, B. Bilge;
Sayar, Ceyhan;
Toksoy, Güven;
Elçioğlu, Nursel

Publication type:

Article

Ameloblastic Fibro-Odontoma of the Maxilla in a Pierre-Robin Sequence Patient.

Published in:

2017

By:

Kufta, Kenneth;
Kang, Steve;
Alawi, Faizan;
Moran, Anna;
Panchal, Neeraj

Publication type:

Case Study

Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both Fetuses.

Published in:

Fetal & Pediatric Pathology, 2016, v. 35, n. 5, p. 339, doi. 10.1080/15513815.2016.1188870

By:

Inan, Cihan;
Sayın, N. Cenk;
Atlı, Emine;
Ulusal, Selma;
Erzincan, Selen;
Uzun, Isil;
Gurkan, Hakan;
Varol, Füsun G.

Publication type:

Article

An Unusual Case of Trisomy 18 Associated with Paucity of Bile Ducts.

Published in:

Fetal & Pediatric Pathology, 2013, v. 32, n. 5, p. 337, doi. 10.3109/15513815.2013.768736

By:

Kahramaner, Zelal;
Erdemir, Aydin;
Cosar, Hese;
Turkoglu, Ebru;
Sutcuoglu, Sumer;
Turelik, Ozlem;
Cumurcu, Suheyla;
Bayol, Umit;
Ozer, Esra

Publication type:

Article

Hajdu-Cheney syndrome - a rare cause of micrognathia.

Published in:

2016

By:

Deepak Amalnath, S.;
Babu, Vinod

Publication type:

Case Study

Goldenhar syndrome with unusual features.

Published in:

Indian Journal of Dermatology, Venereology & Leprology, 2008, v. 74, n. 3, p. 254, doi. 10.4103/0378-6323.41374

By:

Mehta, Bijal;
Nayak, Chitra;
Savant, Shankar;
Amladi, Sangeeta

Publication type:

Article

Evidence in a Human Fetus of Micrognathia and Cleft Lip as Potential Effects of Early Cytomegalovirus Infection.

Published in:

Fetal Diagnosis & Therapy, 2010, v. 28, n. 4, p. 225, doi. 10.1159/000320203

By:

Weichert, Alexander;
Vogt, Markus;
Dudenhausen, Joachim W.;
Kalache, Karim D.

Publication type:

Article

Severe Micrognathia: Indications for EXIT-to-Airway.

Published in:

Fetal Diagnosis & Therapy, 2009, v. 26, n. 3, p. 162, doi. 10.1159/000240162

By:

Morris, Lee M.;
Lim, Foong-Yen;
Elluru, Ravindhra G.;
Hopkin, Robert J.;
Jaekle, Ronald K.;
Polzin, William J.;
Crombleholme, Timothy M.

Publication type:

Article

Diprosopus Associated with Neural Tube Defect and Facial Cleft in the First Trimester.

Published in:

Fetal Diagnosis & Therapy, 2004, v. 19, n. 3, p. 246, doi. 10.1159/000076706

By:

Bulbul, Y.;
Drummond, C. L.;
Hillion, Y.;
Bidat, L.;
Ville, Y.

Publication type:

Article

Prenatal Diagnosis of Double Autosomal Mosaicism (47,XX,+8/47,XX,+14): Phenotype and Molecular Cytogenetic Analysis on Different Tissues.

Published in:

Fetal Diagnosis & Therapy, 2003, v. 18, n. 1, p. 29, doi. 10.1159/000066380

By:

J.K.B. Matheson;
V.A. Matheson;
M. McCorquodale;
J. Santolaya-Forgas

Publication type:

Article

Umbilical Cord Pseudocyst in a Fetus with Trisomy 18.

Published in:

Fetal Diagnosis & Therapy, 2003, v. 18, n. 1, p. 8, doi. 10.1159/000066376

By:

T. Kuwata;
S. Matsubara;
A. Izumi;
K. Odagiri;
T. Tsunoda;
T. Watanabe;
N. Taniguchi;
I. Sato

Publication type:

Article

Construction of fetal inferior facial angle and hemi-mandible length reference ranges at 18-21 weeks' gestation in an Australian population.

Published in:

Australasian Journal of Ultrasound in Medicine, 2017, v. 20, n. 4, p. 168, doi. 10.1002/ajum.12066

By:

Qiu, Robert;
MacKinlay, Katie;
Suen, Melissa;
McLennan, Andrew

Publication type:

Article

Difficult airway associated with bifid glottis and coexistent subglottic stenosis in a patient with Pallister–Hall syndrome: a case report.

Published in:

2018

By:

Oe, Yukimura;
Godai, Kohei;
Masuda, Mina;
Kanmura, Yuichi

Publication type:

Case Study

Successful airway management using a MultiViewScope handle with a stylet scope in a patient with Schwartz-Jampel syndrome.

Published in:

JA Clinical Reports, 2016, v. 2, n. 1, p. 1, doi. 10.1186/s40981-016-0062-5

By:

Mukaihara, Keika;
Godai, Kohei;
Yamada, Tomotsugu;
Hasegawa-Moriyama, Maiko;
Kanmura, Yuichi

Publication type:

Article

Treatment of severe micrognathia in an adult with distraction osteogenesis: A case report.

Published in:

2023

By:

Sekido, Katsuhisa;
Fujiwara, Kumiko;
Tachinami, Hidetake;
Imaue, Shuichi;
Hanashiro, Keishi;
Noguchi, Makoto

Publication type:

Case Study

Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly.

Published in:

2023

By:

Mlay, Kenneth;
Chussi, Desderius;
Mtenga, Philbert;
Shija, Peter;
Msele, Angela

Publication type:

Case Study

Analysis of micrognathia with obstructive sleep apnea syndrome improved by a combination of Le Fort I with horseshoe osteotomies, mandibular distraction osteogenesis, and genioplasty.

Published in:

2022

By:

Koshinuma, Shinya;
Fujii, Takafumi;
Okamura, Takeshi;
Asada, Yasuyuki;
Machida, Yoshisato;
Yamamoto, Gaku

Publication type:

Case Study

Modified ex utero intrapartum treatment procedure in a bicornuate uterus breech presentation Pierre Robin fetus with severe micrognathia and cleft palate.

Published in:

2018

By:

Duek, Irit;
Gil, Ziv;
Solt, Ido

Publication type:

Case Study

Predictive Factors for Perinatal Outcomes of Infants Diagnosed With Micrognathia Antenatally.

Published in:

ENT: Ear, Nose & Throat Journal, 2021, v. 100, n. 1, p. NP16, doi. 10.1177/0145561319855641

By:

Tay, Sok Yan;
Krishnasarma, Rekha;
Mehta, Deepak;
Mehollin-Ray, Amy;
Chandy, Binoy

Publication type:

Article

Trps1 Regulates Development of Craniofacial Skeleton and Is Required for the Initiation of Palatal Shelves Fusion.

Published in:

Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00513

By:

Cho, Kah Yan;
Kelley, Brian P.;
Monier, Daisy;
Lee, Brendan;
Szabo-Rogers, Heather;
Napierala, Dobrawa

Publication type:

Article

Síndrome perisilviano bilateral congénito asociado a secuencia de Pierre Robin: Reporte de caso.

Published in:

Iatreia, 2025, v. 38, n. 1, p. 158, doi. 10.17533/udea.iatreia.279

By:

César Castro-Murillo, Julio;
Leticia Gómez-Guzmán, Enid;
A. Rojas-Cerón, Christian

Publication type:

Article

Inactivation of Fam20b in the neural crest‐derived mesenchyme of mouse causes multiple craniofacial defects.

Published in:

European Journal of Oral Sciences, 2018, v. 126, n. 5, p. 433, doi. 10.1111/eos.12563

By:

Liu, Xuenan;
Li, Nan;
Zhang, Hua;
Liu, Jing;
Zhou, Nan;
Ran, Chunxiao;
Chen, Xiaoyan;
Lu, Yongbo;
Wang, Xiaofang;
Qin, Chunlin;
Xiao, Jing;
Liu, Chao

Publication type:

Article

Comparable Low-Level Mosaicism in Affected and Non Affected Tissue of a Complex CDH Patient.

Published in:

PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0015348

By:

Veenma, Danielle;
Beurskens, Niels;
Douben, Hannie;
Eussen, Bert;
Noomen, Petra;
Govaerts, Lutgarde;
Grijseels, Els;
Lequin, Maarten;
de Krijger, Ronald;
Tibboel, Dick;
de Klein, Annelies;
Van Opstal, Dian

Publication type:

Article

Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22.

Published in:

Acta Medica Iranica, 2015, v. 53, n. 12, p. 782

By:

Mosallanejad, Asieh;
Sayarifard, Fatemeh;
Hosseinverdi, Sima;
Abbasi, Farzaneh;
Mirzaee, Hosein Shabni;
Rezaei, Nima

Publication type:

Article

Orthodontic Treatment in Conjunction with Twin-bock Treatment and Growth Hormone Therapy in Silver Russell Syndrome.

Published in:

2017

By:

Ko, Su-Jin;
Seo, Ji Young;
Kwon, Yong-Dae;
Cheon, Kyounga;
Park, Jae Hyun

Publication type:

journal article

Orofaciodigital (OFD) syndromes: Report of a case with OFDS type I.

Published in:

Hellenic Orthodontic Review, 2010, v. 13, n. 1/2, p. 43

By:

Papagrigorakis, Manolis I.;
Fotos, Spyros;
Damanakis, Geogrios;
Lygidakis, Nikolaos;
Lysikatos, Nikolaos;
Synodinos, Filippos

Publication type:

Article

Barx1 is necessary for zebrafish cranial neural crest patterning and pharyngeal arch chondrogenesis.

Published in:

FASEB Journal, 2007, v. 21, n. 6, p. A970, doi. 10.1096/fasebj.21.6.a970-c

By:

Sperber, Steven;
Dawid, Igor

Publication type:

Article

Students, blood and teeth.

Published in:

2015

By:

Youngs, Robin;
Fisher, Edward

Publication type:

Editorial

Total Absence of Ribs in a Newborn with Cerebrocostomandibular Syndrome.

Published in:

Pediatric & Developmental Pathology, 2011, v. 14, n. 2, p. 134, doi. 10.2350/09-11-0745-CR.1

By:

LALE, SEEMA;
ARDINGER, HOLLY;
MARDIS, NEIL;
CHANGHO, SHEELAH;
LANCASTER, THOMAS;
SINGH, VIVEKANAND

Publication type:

Article

Biochemical Abnormality Associated with Smith-Lemli-Opitz Syndrome in an Infant with Features of Rutledge Multiple Congenital Anomaly Syndrome Confirms that the Latter Is a Variant of the Former.

Published in:

Pediatric & Developmental Pathology, 2003, v. 6, n. 3, p. 270, doi. 10.1007/s10024-002-1116-4

By:

Rakheja, Dinesh;
Wilson, Golder N.;
Rogers, Beverly B.

Publication type:

Article

Pontine hypoplasia in cri-du-chat syndrome: alterations in diffusion tensor imaging.

Published in:

2017

By:

Corrêa, Diogo;
Ventura, Nina;
Gasparetto, Emerson

Publication type:

Letter