Works matching DE "MICROGNATHIA"

Results: 285

Immediate postdelivery airway management of neonates with prenatally diagnosed micrognathia: A retrospective observational study.

Published in:

Pediatric Anesthesia, 2024, v. 34, n. 3, p. 267, doi. 10.1111/pan.14806

By:

Berger, Jessica A.;
Nelson, Olivia;
Staben, James;
Javia, Luv R.;
Simpao, Allan F.;
Khalek, Nahla;
Oliver, Edward R.;
Adzick, N. Scott;
Lin, Elaina E.

Publication type:

Article

Two infants with presumed Zika congenital syndrome presenting for exam under general anesthesia.

Published in:

Pediatric Anesthesia, 2017, v. 27, n. 8, p. 868, doi. 10.1111/pan.13186

By:

Kuntz, Michael T.;
Tutiven, Jacqueline L.;
Read, Sarah Parker;
Ventura, Camila V.;
Berrocal, Audina M.

Publication type:

Article

Features of lateral cephalograms associated with difficult laryngoscopy in Japanese children undergoing oral and maxillofacial surgery.

Published in:

Pediatric Anesthesia, 2013, v. 23, n. 11, p. 994, doi. 10.1111/pan.12178

By:

Kohjitani, Atsushi;
Miyawaki, Takuya;
Miyawaki, Shouichi;
Nakamura, Norifumi;
Iwase, Yoko;
Nishihara, Kazuhide;
Ohno, Sachi;
Shimada, Masahiko;
Sugiyama, Kazuna

Publication type:

Article

Arytenoid prolapse and inability to ventilate.

Published in:

Pediatric Anesthesia, 2013, v. 23, n. 9, p. 876, doi. 10.1111/pan.12221

By:

Patino, Mario;
Hart, Catherine K.;
Mahmoud, Mohamed

Publication type:

Article

Ultrasonographic study of fetal mandibular markers during the first trimester in a Chinese population.

Published in:

Journal of Obstetrics & Gynaecology Research, 2022, v. 48, n. 2, p. 333, doi. 10.1111/jog.15121

By:

Li, Hezhou;
Zhu, Zhengfeng

Publication type:

Article

Prenatal Diagnosis of Gómez-López-Hernández Syndrome.

Published in:

Fetal Diagnosis & Therapy, 2023, v. 50, n. 2, p. 92, doi. 10.1159/000530643

By:

Pomar, Leo;
Rieder, Wawrzyniec;
Dubruc, Estelle;
Giuliano, Fabienne;
Atallah, Isis;
Lebon, Sébastien;
Vial, Yvan

Publication type:

Article

Kabuki syndrome: a case report.

Published in:

Journal of Orthodontics, 2006, v. 33, n. 4, p. 242, doi. 10.1179/146531205225021717

By:

Lung, Z. H. S.;
Rennie, A.

Publication type:

Article

EMANUEL SYNDROME (ES): NEW CASE-REPORT AND REVIEW OF THE LITERATURE.

Published in:

2015

By:

Jancevska, Snezana;
Kitanovski, Mile;
Laban, Nevenka;
Danilovski, Dragan;
Tasic, Velibor;
Gucev, Zoran S.

Publication type:

Case Study

Unanticipated difficult intubation in a child with Beals-Hecht syndrome presenting for emergency surgery.

Published in:

2015

By:

Kalra, S.

Publication type:

Case Study

Solitary median maxillary central incisor syndrome occurring together with oromandibular-limb hypogenesis syndrome type 1: a case report of this previously unreported combination of syndromes.

Published in:

International Journal of Paediatric Dentistry, 2008, v. 18, n. 4, p. 306, doi. 10.1111/j.1365-263X.2007.00907.x

By:

LERTSIRIVORAKUL, JINDA;
HALL, ROGER K.

Publication type:

Article

Anesthetic management of pediatric patients with Emanuel syndrome.

Published in:

Journal of Anesthesia, 2015, v. 29, n. 3, p. 450, doi. 10.1007/s00540-014-1955-y

By:

Nishinarita, Reiko;
Mihara, Takahiro;
Nakamura, Nobuhito;
Miyamoto, Yoshihisa;
Ka, Koui

Publication type:

Article

Early dental management of patients with Mobius syndrome.

Published in:

Oral Diseases, 2006, v. 12, n. 6, p. 533, doi. 10.1111/j.1601-0825.2006.01231.x

By:

Magalhães, MHCG;
Araújo, LCA;
Chiaradia, CC;
Fraige, A;
Zamunaro, MT;
Mantesso, A

Publication type:

Article

A case achieved at 28 weeks of gestation by cervical cerclage with retained placenta after expulsion of nonviable fetus underwent selective termination in multifetal pregnancy.

Published in:

Perinatal Journal / Perinatoloji Dergisi, 2019, v. 27, n. 2, p. 119, doi. 10.2399/prn.19.0272005

By:

Özcan, Pınar;
Kütük, Mehmet Serdar;
Takmaz, Taha;
İşlek, Havva Sevde

Publication type:

Article

Congenital Contractural Arachnodactyly (Beals-Hecht Syndrome): A Case Report.

Published in:

2011

By:

Karaman, Ali;
Kahveci, Hasan

Publication type:

Case Study

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

Seckel syndrome associated with oligodontia, microdontia, enamel hypoplasia, delayed eruption, and dentin dysmineralization: a new variant?

Published in:

Journal of Oral Pathology & Medicine, 2006, v. 35, n. 10, p. 639, doi. 10.1111/j.1600-0714.2006.00462.x

By:

De Coster, P. J.;
Verbeeck, R. M. H.;
Holthaus, V.;
Martens, L. C.;
Vral, A.

Publication type:

Article

Unusual oral findings in dermatosparaxis (Ehlers-Danlos syndrome type VIIC).

Published in:

2003

By:

De Coster, P.J.;
Malfait, F.;
Martens, L.C.;
De Paepe, A.

Publication type:

journal article

Síndrome del cromosoma 21 en anillo: reporte de 2 casos.

Published in:

Revista Medica del IMSS, 2025, v. 63, n. 1, p. 1, doi. 10.5281/zenodo.13381482

By:

Alejandra Guzmán-Santiago, Tania;
Juárez-Melchor, Daniela;
Jiménez-Pérez, Berenice;
Vera-Loaiza, Aurea;
Alberto Pérez-Arzola, Alan;
Hernández-Castañeda, Yazmin;
Omar Rodríguez-Hurtado, Pablo;
Enrique Crisanto-López, Israel;
María Garduño-Zarazúa, Luz;
Salazar-Bonilla, Wilbert

Publication type:

Article

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

Giant Occipital Encephalocele Associated with Microcephaly and Micrognathia.

Published in:

Pediatric Neurosurgery, 2009, v. 44, n. 6, p. 515, doi. 10.1159/000187128

By:

Agrawal, Amit;
Lakhkar, Bhavana B.;
Lakhkar, Bhushan;
Grover, Ankur

Publication type:

Article

Giant Occipital Encephalocele with Microcephaly and Micrognathia.

Published in:

Pediatric Neurosurgery, 2004, v. 40, n. 4, p. 205, doi. 10.1159/000081941

By:

Agrawal, Deepak;
Mahapatra, A. K.

Publication type:

Article

Buphthalmos in trisomy 13.

Published in:

2005

By:

Bunting, R.;
Leitch, J.

Publication type:

Letter

A Rare Case of Hutchınson-Gılford Progerıa Syndrome with Early Dental Loss without Decay.

Published in:

Makara Journal of Health Research, 2018, v. 22, n. 2, p. 63, doi. 10.7454/msk.v22i2.9486

By:

Pekdemir, Tuğçe N.;
Öztürk, Duygu;
Çetindağ, Merve T.;
Akleyn, Ebru;
Sarıyıldız, Cansu O.;
Callea, Michele;
Yavuz, İzzet

Publication type:

Article

Micrognathia as a Diagnosis Marker for the Prenatal Identification of Edwards Syndrome.

Published in:

Biomedicines, 2025, v. 13, n. 3, p. 573, doi. 10.3390/biomedicines13030573

By:

Albu, Cristina-Crenguţa;
Brăila, Anca Daniela;
Poalelungi, Cristian-Viorel;
Bohîltea, Laurenţiu-Camil;
Bănățeanu, Andreea-Mariana;
Damian, Constantin Marian;
Dîră, Laurențiu Mihai;
Bogdan-Andreescu, Claudia Florina

Publication type:

Article

New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 4, p. 224, doi. 10.1007/s100380050077

By:

Tsukahara, M.;
Sugio, Yoshitsugu

Publication type:

Article

Smith-Lemli-Opitz Syndrome: A Case with Annular Pancreas.

Published in:

2014

By:

Demirdöven, Mehmet;
Yazgan, Hamza;
Korkmaz, Mevlit;
Gebeşçe, Arzu;
Tonbul, Alparslan

Publication type:

Case Study

Clinical and radiographic characteristics of pycnodysostosis: A systematic review.

Published in:

Imaging Science in Dentistry, 2024, v. 54, n. 1, p. 13, doi. 10.5624/isd.20230191

By:

Goes Gonzaga, Amanda Katarinny;
de Oliveira Costa, Carla Samily;
de Farias Morais, Hannah Gil;
da Fonseca Neto, Braz;
Pereira Pinto, Leão;
Dantas, Wagner Ranier Maciel;
Teixeira de Oliveira, Patricia;
Pita de Melo, Daniela

Publication type:

Article

A novel mutation in the COL2A1 gene in a patient with Stickler syndrome type 1: a case report and review of the literature.

Published in:

2017

By:

Higuchi, Yousuke;
Hasegawa, Kosei;
Yamashita, Miho;
Tanaka, Hiroyuki;
Tsukahara, Hirokazu

Publication type:

journal article

Report of a Case with Trisomy 9 Mosaicism.

Published in:

Iranian Journal of Medical Sciences, 2016, v. 41, n. 3, p. 249

By:

Miryounesi, Mohammad;
Dianatpour, Mehdi;
Shadmani, Zahra;
Ghafouri-Fard, Soudeh

Publication type:

Article

Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause.

Published in:

Clinical Genetics, 2014, v. 86, n. 3, p. 246, doi. 10.1111/cge.12259

By:

Petit, F.;
Escande, F.;
Jourdain, A.S.;
Porchet, N.;
Amiel, J.;
Doray, B.;
Delrue, M.A.;
Flori, E.;
Kim, C.A.;
Marlin, S.;
Robertson, S.P.;
Manouvrier‐Hanu, S.;
Holder‐Espinasse, M.

Publication type:

Article

Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 8, p. 1062, doi. 10.1038/ejhg.2014.234

By:

Kagami, Masayo;
Mizuno, Seiji;
Matsubara, Keiko;
Nakabayashi, Kazuhiko;
Sano, Shinichiro;
Fuke, Tomoko;
Fukami, Maki;
Ogata, Tsutomu

Publication type:

Article

Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 4, p. 481, doi. 10.1038/ejhg.2014.132

By:

Romanelli Tavares, Vanessa L;
Gordon, Christopher T;
Zechi-Ceide, Roseli M;
Kokitsu-Nakata, Nancy Mizue;
Voisin, Norine;
Tan, Tiong Y;
Heggie, Andrew A;
Vendramini-Pittoli, Siulan;
Propst, Evan J;
Papsin, Blake C;
Torres, Tatiana T;
Buermans, Henk;
Capelo, Luciane Portas;
den Dunnen, Johan T;
Guion-Almeida, Maria L;
Lyonnet, Stanislas;
Amiel, Jeanne;
Passos-Bueno, Maria Rita

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

Case report of schizophrenia in adolescent with Russell- Silver syndrome.

Published in:

Psychiatry & Clinical Neurosciences, 2014, v. 68, n. 7, p. 582, doi. 10.1111/pcn.12169

By:

Inoue, Katsuo;
Natsuyama, Takashi;
Miyaoka, Hitoshi

Publication type:

Article

Three-dimensional sonographic visualization of fetal facial anomaly.

Published in:

Acta Obstetricia et Gynecologica Scandinavica, 1999, v. 78, n. 10, p. 917

By:

Manabe, Atsushi;
Hata, Toshiyuki;
Aoki, Showa;
Matsumoto, Minako;
Yanagihara, Toshihiro;
Yamada, Yohko;
Irikoma, Shingo;
Miyazaki, Kohji

Publication type:

Article

Craniofacial growth disturbance is related to temporomandibular joint abnormality in patients with juvenile idiopathic arthritis, but normal facial profile was also found at the 27-year follow-up.

Published in:

Scandinavian Journal of Rheumatology, 2010, v. 39, n. 5, p. 373, doi. 10.3109/03009741003685624

By:

Arvidsson, LZ;
Fjeld, MG;
Smith, H-J;
Flatø, B;
Øgaard, B;
Larheim, TA

Publication type:

Article

Students, blood and teeth.

Published in:

2015

By:

Youngs, Robin;
Fisher, Edward

Publication type:

Editorial

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

Maturation of ureter-bladder connection in mice is controlled by LAR family receptor protein tyrosine phosphatases.

Published in:

2009

By:

Uetani, Noriko;
Bertozzi, Kristen;
Chagnon, Melanie J.;
Hendriks, Wiljan;
Tremblay, Michel L.;
Bouchard, Maxime

Publication type:

journal article

A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation.

Published in:

2006

By:

Yang, Shao H.;
Meta, Margarita;
Xin Qiao;
Frost, David;
Bauch, Joy;
Coffinier, Catherine;
Majumdar, Sharmila;
Bergo, Martin O.;
Young, Stephen G.;
Fong, Loren G.;
Qiao, Xin

Publication type:

journal article

Freeman-Sheldon syndrome with cerebral venous thrombosis: Is it a coincidence?

Published in:

Journal of Postgraduate Medicine, 2010, v. 56, n. 1, p. 37, doi. 10.4103/0022-3859.62428

By:

Al-Sajee, D. M.;
Habbal, O. A.;
Reyes, Z. S.

Publication type:

Article

Prenatal diagnosis and findings of tetrasomy 9p.

Published in:

Journal of Obstetrics & Gynaecology Research, 2015, v. 41, n. 7, p. 997, doi. 10.1111/jog.12706

By:

Lazebnik, Noam;
Cohen, Leslie

Publication type:

Article

Successful ex utero intrapartum treatment procedure for prenatally diagnosed severe micrognathia: A case report.

Published in:

Journal of Obstetrics & Gynaecology Research, 2014, v. 40, n. 8, p. 2005, doi. 10.1111/jog.12423

By:

Suenaga, Masanori;
Hidaka, Nobuhiro;
Kido, Saki;
Otera, Yuka;
Fukushima, Kotaro;
Kato, Kiyoko

Publication type:

Article

Prenatal diagnosis and tridimensional ultrasound features of bilateral femoral hypoplasia - Unusual facies syndrome.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2009, v. 22, n. 10, p. 936, doi. 10.1080/14767050902994606

By:

Figueroa, Cecilia;
Plasencia, Walter;
Eguiluz, Idoya;
De Luis, Maria;
Barber, Miguel A.;
Valle, Leonor;
García-Hernández, Jose A.

Publication type:

Article

Mandibular Distraction in Robin Sequence – A Systematic Review of Morphologic Changes and Implications for Long-Term Growth.

Published in:

FACE (2732-5016), 2024, v. 5, n. 3, p. 491, doi. 10.1177/27325016241255141

By:

Prescher, Hannes;
Nathan, Shelby L.;
Ghosh, Kanad;
Henderson, Charlotte;
Reid, Russell R.

Publication type:

Article

Unveiling a Misdiagnosed Midline Cervical Cleft: A Case Report and Review of the Literature.

Published in:

2024

By:

Rezania, Nikki;
O'Neill, Elizabeth S.;
Harmon, Kelly A.;
Arnold, Sydney H.;
Tragos, Christina

Publication type:

Case Study

First-trimester detection of micrognathia as a presentation of mandibulofacial dysostosis with microcephaly.

Published in:

Journal of Obstetrics & Gynaecology, 2021, v. 41, n. 5, p. 821, doi. 10.1080/01443615.2020.1785410

By:

Xu, Bi-Qiu;
Zhen, Li;
Li, Dong-Zhi

Publication type:

Article

Prenatal ultrasound diagnosis of Tessier number 7 cleft: Case report and review of the literature.

Published in:

2017

By:

Cavaco-Gomes, João;
Duarte, Carla;
Pereira, Elsa;
Matias, Alexandra;
Montenegro, Nuno;
Merz, Eberhard

Publication type:

journal article