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1950 1
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1997 1
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2007 1
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14 results

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Page 1
Fetal Micro and Macroglossia: Defining Normal Fetal Tongue Size.
Koren N, Shust-Barequet S, Weissbach T, Raviv O, Abu Snenh S, Abraham E, Cahan T, Eisenberg V, Yulzari V, Hadi E, Adamo L, Mazaki Tovi S, Achiron R, Kivilevitch Z, Weisz B, Kassif E. Koren N, et al. J Ultrasound Med. 2023 Jan;42(1):59-70. doi: 10.1002/jum.15983. Epub 2022 Apr 9. J Ultrasound Med. 2023. PMID: 35396717
Using the new charts, we were able to identify 2 cases of macroglossia, subsequently diagnosed with Beckwith-Wiedemann, and 4 cases of microglossia, 3 associated with Pierre-Robin sequence, and 1 associated with persistent buccopharyngeal membrane. ...
Using the new charts, we were able to identify 2 cases of macroglossia, subsequently diagnosed with Beckwith-Wiedemann, and 4 cases of mi …
Prenatal detection of deletion 6q13q15 in a complex karyotype.
Yu M, Obringer AC, Fowler MH, Hummel M, Wenger SL. Yu M, et al. Prenat Diagn. 2005 Dec;25(12):1084-7. doi: 10.1002/pd.1265. Prenat Diagn. 2005. PMID: 16231325 Review.
The infant presented with multiple congenital anomalies, primarily limited to the head and neck, including hypertelorism, broad nose, micrognathia, cleft palate, microglossia and low-set ears with microtia. METHODS: Amniocytes of the fetus and blood of the patient and her …
The infant presented with multiple congenital anomalies, primarily limited to the head and neck, including hypertelorism, broad nose, microg …
Mobius sequence--a Swedish multidiscipline study.
Strömland K, Sjögreen L, Miller M, Gillberg C, Wentz E, Johansson M, Nylén O, Danielsson A, Jacobsson C, Andersson J, Fernell E. Strömland K, et al. Eur J Paediatr Neurol. 2002;6(1):35-45. doi: 10.1053/ejpn.2001.0540. Eur J Paediatr Neurol. 2002. PMID: 11993954
Obvious associated systemic anomalies observed included: limb malformations (10), Poland anomaly (2), hypodontia (7), microglossia (6), cleft palate (4), hearing impairment (5) and external ear malformation (1). ...
Obvious associated systemic anomalies observed included: limb malformations (10), Poland anomaly (2), hypodontia (7), microglossia (6 …
Transmission of the dysgnathia complex from mother to daughter.
Erlich MS, Cunningham ML, Hudgins L. Erlich MS, et al. Am J Med Genet. 2000 Nov 27;95(3):269-74. Am J Med Genet. 2000. PMID: 11102934
We report the first observation of parent-to-child transmission of dysgnathia, a rare disorder characterized by severe mandibular hypoplasia or agenesis, ear anomalies, microstomia, and microglossia. Patient 1 was noted prenatally by ultrasound to have severe micrognathia …
We report the first observation of parent-to-child transmission of dysgnathia, a rare disorder characterized by severe mandibular hypoplasia …
Prevalence of tongue lesions among Turkish schoolchildren.
Ugar-Cankal D, Denizci S, Hocaoglu T. Ugar-Cankal D, et al. Saudi Med J. 2005 Dec;26(12):1962-7. Saudi Med J. 2005. PMID: 16380783
We examined all the children for the presence of the following tongue lesions: 1) ankyloglossia, 2) bifid tongue, 3) fissured tongue, 4) geographic tongue, 5) median rhomboid glossitis, 6) lingual thyroid nodule, 7) atrophic tongue, 8) hairy tongue, 9) crenation tongue, 10) furre …
We examined all the children for the presence of the following tongue lesions: 1) ankyloglossia, 2) bifid tongue, 3) fissured tongue, 4) geo …
Development of speech, feeding, eating, and facial expression in Möbius sequence.
Sjögreen L, Andersson-Norinder J, Jacobsson C. Sjögreen L, et al. Int J Pediatr Otorhinolaryngol. 2001 Sep 28;60(3):197-204. doi: 10.1016/s0165-5876(01)00532-8. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11551610
Observed orofacial anomalies were tongue dysfunction (16), micrognatia (8), microglossia (7), cleft palate (4), and cleft lip (1). Seventeen had speech problems, 16 reported feeding difficulties in infancy, 14 eating problems, and 8 drooling. ...
Observed orofacial anomalies were tongue dysfunction (16), micrognatia (8), microglossia (7), cleft palate (4), and cleft lip (1). Se …
Optic nerve coloboma, Dandy-Walker malformation, microglossia, tongue hamartomata, cleft palate and apneic spells: an existing oral-facial-digital syndrome or a new variant?
Toriello HV, Lemire EG. Toriello HV, et al. Clin Dysmorphol. 2002 Jan;11(1):19-23. doi: 10.1097/00019605-200201000-00004. Clin Dysmorphol. 2002. PMID: 11822700
We report on a female infant with postaxial polydactyly of the hands, preaxial polydactyly of the right foot, cleft palate, microglossia and tongue hamartomata consistent with an oral-facial-digital syndrome (OFDS). ...
We report on a female infant with postaxial polydactyly of the hands, preaxial polydactyly of the right foot, cleft palate, microglossia …
Airway management during an EXIT procedure for a fetus with dysgnathia complex.
Baker PA, Aftimos S, Anderson BJ. Baker PA, et al. Paediatr Anaesth. 2004 Sep;14(9):781-6. doi: 10.1111/j.1460-9592.2004.01284.x. Paediatr Anaesth. 2004. PMID: 15330963
Nonsyndromal dysgnathia is a rare disorder with a probable genetic basis characterized by a hypoplastic or absent mandible (agnathia), microstomia, microglossia, and ear anomalies secondary to a defect in the ventral portion of the first branchial arch caused by defective …
Nonsyndromal dysgnathia is a rare disorder with a probable genetic basis characterized by a hypoplastic or absent mandible (agnathia), micro …
Severe Agnathia-Otocephaly Complex: Surgical Management and Longitudinal Follow-up From Birth Through Adulthood.
Golinko MS, Shetye P, Flores RL, Staffenberg DA. Golinko MS, et al. J Craniofac Surg. 2015 Nov;26(8):2387-92. doi: 10.1097/SCS.0000000000002150. J Craniofac Surg. 2015. PMID: 26517463
Agnathia-otocephaly complex (AOC) is characterized by mandibular hypo- or aplasia, ear abnormalities, microstomia, and microglossia. Though rare and often fatal, this is the first report detailing various reconstructive strategies beyond infancy as well as longitudinal fol …
Agnathia-otocephaly complex (AOC) is characterized by mandibular hypo- or aplasia, ear abnormalities, microstomia, and microglossia. …
Development of the fetal tongue between 14 and 26 weeks of gestation: in utero ultrasonographic measurements.
Achiron R, Ben Arie A, Gabbay U, Mashiach S, Rotstein Z, Lipitz S. Achiron R, et al. Ultrasound Obstet Gynecol. 1997 Jan;9(1):39-41. doi: 10.1046/j.1469-0705.1997.09010039.x. Ultrasound Obstet Gynecol. 1997. PMID: 9060129 Free article.
During the study period we evaluated two cases with tongue circumference outside these 95% confidence limits: one had microglossia, the other macroglossia, and both were found to be associated with abnormal fetal karyotype. ...
During the study period we evaluated two cases with tongue circumference outside these 95% confidence limits: one had microglossia, t …
14 results