A Rare Association of Monosomy 18 with Translocation 13p 11/
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Monosomy 18p is a rare chromosomal disorder in which all or part of the short arm (p) of chromosome 18 is deleted (monosomic). The disorder is typically characterized by short stature, variable degrees of mental retardation, speech delays, malformations of the skull and facial (craniofacial) region, and/or additional physical abnormalities. We report monosomy 18 with translocation 13p 11/18 with Cholelithiasis in a 8 year old girl who presented with acute right hypochondriac pain with fever. This association has never been reported in this age group. This case report highlights this rare association which a clinician should keep in mind while dealing with this disorder....

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