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.

Micrognathia

Developmental hypoplasia of the mandible.


Total: 6

                       


(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.
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.
11152148
 FEMALE Infant
Situs inversus totalis and congenital hypoglossia.
Amor DJ, Craig JE.
Clin Dysmorphol. 2001;10(1):47-50.
We describe a female infant with congenital hypoglossia, micrognathia 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 case of lingual agenesis associated with micrognathia and situs inversus is reported in a newborn presenting with upper airway obstruction at birth.