Situs inversus totalis

A rare, genetic, developmental defect during embryogenesis characterized by total mirror-image transposition of both thoracic and abdominal viscera across the left-right axis of the body. Congenital abnormalities, such as primary ciliary dyskinesia, Kartagener type, polysplenia syndrome, biliary atresia, congenital heart disease, and midgut malrotation, as well as vascular anomalies (e.g. absence of retrohepatic inferior vena cava, preduodenal portal vein, aberrant hepatic arterial anatomy) and malignancy, are frequently associated.

Aglossia

Absence of the tongue owing to a developmental abnormality.

Total: 11

(per page)

PMID (PMCID)
28610820	MALE	Child
	Mandibular symphyseal midline distraction osteogenesis for micrognathia associated with aglossia and situs inversus totalis.
	Ren XC, Li YF, Liu Y, Zhu SS. Int J Oral Maxillofac Surg. 2017;46(10):1346-1351.
	In a review of the literature, this is the first case of micrognathia associated with aglossia and situs inversus totalis that has been treated by mandibular symphyseal midline distraction osteogenesis for the dentofacial deformity.
28610820	MALE	Child
	Mandibular symphyseal midline distraction osteogenesis for micrognathia associated with aglossia and situs inversus totalis.
	Ren XC, Li YF, Liu Y, Zhu SS. Int J Oral Maxillofac Surg. 2017;46(10):1346-1351.
	Mandibular symphyseal midline distraction osteogenesis for micrognathia associated with aglossia and situs inversus totalis.
28610820	MALE	Child
	Mandibular symphyseal midline distraction osteogenesis for micrognathia associated with aglossia and situs inversus totalis.
	Ren XC, Li YF, Liu Y, Zhu SS. Int J Oral Maxillofac Surg. 2017;46(10):1346-1351.
	This report describes the case of a 7-year-old boy suffering from micrognathia, aglossia, and situs inversus totalis simultaneously, and the treatment for his micrognathia by mandibular symphyseal midline distraction osteogenesis, guided by virtual surgical planning and a three-dimensional printed surgical template.
26349289	MALE	Adult
	Multidisciplinary Rehabilitation in a Case of Congenital Aglossia with Situs Inversus Totalis.
	Tripathi T, Neha , Gill S, Rai P. Int J Orthod Milwaukee. 2015;26(2):39-43.
	Multidisciplinary Rehabilitation in a Case of Congenital Aglossia with Situs Inversus Totalis.
26349289	MALE	Adult
	Multidisciplinary Rehabilitation in a Case of Congenital Aglossia with Situs Inversus Totalis.
	Tripathi T, Neha , Gill S, Rai P. Int J Orthod Milwaukee. 2015;26(2):39-43.
	The present case report describes multidisciplinary rehabilitation in a patient with Aglossia Congenita along with dextrocardia, situs inversus, mutilated dentition with a lack of occlusal table and compromised esthetics.
18280945	FEMALE
	Complete and isolated congenital aglossia: case report and treatment of sequelae using rapid prototyping models.
	Salles F, Anchieta M, Costa Bezerra P, Torres ML, Queiroz E, Faber J. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008;105(3):e41-7.
	Most cases of aglossia and hypoglossia reported in the literature were associated with limb deformities, cleft palate, deafness, situs inversus, and several syndromes, such as Moebius, Pierre Robin, and Hanhart.
11152148	FEMALE	Infant
	Situs inversus totalis and congenital hypoglossia.
	Amor DJ, Craig JE. Clin Dysmorphol. 2001;10(1):47-50.
	Situs inversus-hypoglossia falls into a spectrum of aetiologically non-specific developmental field defects that includes the Aglossia-adactylia spectrum and the Agnathia-holoprosencephaly spectrum.
9142661 (3054266)	FEMALE	Infant, Newborn
	Congenital aglossia with situs inversus totalis--a case report.
	Jang GY, Lee KC, Choung JT, Son CS, Tockgo YC. J Korean Med Sci. 1997;12(1):55-7.
	We experienced a case of congenital aglossia with situs inversus in a female infant aged twelve days.
9142661 (3054266)	FEMALE	Infant, Newborn
	Congenital aglossia with situs inversus totalis--a case report.
	Jang GY, Lee KC, Choung JT, Son CS, Tockgo YC. J Korean Med Sci. 1997;12(1):55-7.
	Congenital aglossia with situs inversus totalis--a case report.
2197246	MALE	Infant, Newborn
	Congenital aglossia and situs inversus.
	Dunham ME, Austin TL. Int J Pediatr Otorhinolaryngol. 1990;19(2):163-8.
	Congenital aglossia and situs inversus.
2197246	MALE	Infant, Newborn
	Congenital aglossia and situs inversus.
	Dunham ME, Austin TL. Int J Pediatr Otorhinolaryngol. 1990;19(2):163-8.
	A review of the literature reveals two previously reported cases of congenital aglossia and situs inversus.