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Acrofacial dysostosis Rodriguez type (disorder)
Acrofacial dysostosis Rodriguez type
A multiple malformation syndrome in which mandibulofacial dysostosis and severe limb reduction defects are associated with complex malformations of different organs and systems especially the central nervous system, urogenital tract, heart, and lungs. The mandibulofacial defect causes death by respiratory distress. Limb reduction is severe and includes shoulder and pelvis hypoplasia, phocomelia with humerus hypoplasia, absent radius and ulna, complete absence of long bones of the legs, and various hand anomalies, predominantly preaxial reduction. These infants also show facial dysmorphism and ear anomalies. The condition is a rare with an autosomal recessive mode of inheritance. The prognosis is poor and this condition leads to death in utero or shortly after birth.
acrofaciale dysostose Rodriguez-type
Id720430002
StatusPrimitive
Associated morphologyDysplasia
Finding siteBone structure of extremity
Finding siteBone structure of extremity
OccurrenceCongenital
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyAbnormal shortening
Finding siteEntire limb
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDysplasia
Finding siteBone structure of face
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0
CorrelationSNOMED CT source code to target map code correlation not specified