Majewski Syndrome, Short Rib Polydactyly Syndrome (SRPS) Type II - A Rare Case Report, with Review of Literature
Journal Title: Journal of Advances in Medicine and Medical Research - Year 2015, Vol 9, Issue 12
Abstract
Short Rib Polydactyly Syndrome (SRPS) type II also known as Majewski syndrome, is the rarest of the four subtypes of SRPS which is a rare inherited skeletal dysplasia. We report a case of Majewski syndrome in a neonate with brief review of literature. A 24 years old primigravida, with history of second degree consanguineous marriage underwent a Prenatal USG which revealed anhydramnios, bilateral enlarged kidneys, extremely narrow thorax and bilateral short limbs with polydactyly. Based on these findings a probable diagnosis of lethal skeletal dysplasia was made and termination of pregnancy advised. Refusing termination the mother delivered a male foetus at 30 weeks with severe respiratory distress and gross anomalies. The foetus succumbed to respiratory failure inspite of resuscitation. Gross findings were a male foetus with enlarged head, hydropic face, hypertelorism, short nose, depressed nasal bridge, pseudo cleft lip, cleft palate, low set posterior rotated ears, cystic hygroma, micrognathia, short and narrow chest, all the limbs showed mesomelic limb shortening, postaxial polydactyly, syndactyly and brachydactyly. Postnatal X-ray, CT scan and USG confirmed the above mentioned features and additional findings were extremely short horizontal ribs and disproportionately shortened ovoid tibia. Autopsy revealed a bell shaped thorax, small hypoplastic lungs, bilateral enlarged kidneys, atrial septal defect, hypoplastic epiglottis and larynx and short small intestine. Microscopic findings of pulmonary hypoplasia, renal cystic dysplasia, hepatic fibrosis and markedly retarded endochondral ossification correlate with the clinical, radiological and pathological findings of Short Rib Polydactyly Syndrome Type II -Majewski Syndrome.
Authors and Affiliations
Sainath K. Andola, Rajashree J. Ingin, Dimple Mehrotra, Radhamohan Rana
Two Sisters with Leukoencephalopathy, Hearing Loss and Retinopathy: A Familial Case of Susac's Syndrome?
Aims: Susac’s syndrome is a rare clinical entity characterized by encephalopathy, sensorineural hearing loss and retinopathy caused by immune-mediated arteriole occlusion in the brain, retina and inner ear. No familial c...
Endodontic Management of C-shaped Canals in Mandibular Second Molars
Aim: C shaped canal, a common root canal variation in mandibular molars mandates thorough identification and management, when present. Of the several known configurations of C-shaped canals, one often seen is the root ca...
The Effect of Denitrification in the Human Dental Biofilm on Oral Tissues
Global oral health surveys reveal that periodontal disease and dental caries affect human populations throughout the world. Denitrification plays both positive and negative roles in these disease processes by producing b...
Rheological and Microcirculation System Disorders in Experimental Hyperthyroidism
Parameters of activity of peripheral blood supply system of the liver and kidneys in interrelation with rheological functions of blood during an experimental hyperthyroidism have been studied. Disorders of rheological fu...
Outcome and Congenital Anomalies in Children Born after Assisted Reproductive Technology in Port Harcourt
Aim: To evaluate the outcome of children born following Assisted Reproductive Technology in Port Harcourt, Nigeria. Study Design: A retrospective study. Place of Study: Department of Paediatrics, University of Port Harco...