Road to a rare diagnosis: Description of novel unbalanced translocation causing partial trisomy 17p

Melab Musabi; Ayman Saker; Jessi Baer; Peter Wang; Anahita Mohseni Meybodi; Chitra Prasad; Soume Bhattacharya

doi:10.1002/ccr3.6343

Road to a rare diagnosis: Description of novel unbalanced translocation causing partial trisomy 17p

Clin Case Rep. 2022 Oct 6;10(10):e6343. doi: 10.1002/ccr3.6343. eCollection 2022 Oct.

Authors

Melab Musabi¹, Ayman Saker¹, Jessi Baer¹, Peter Wang², Anahita Mohseni Meybodi^{3

4}, Chitra Prasad⁵, Soume Bhattacharya¹

Affiliations

¹ Department of Paediatrics, Neonatal- Perinatal Medicine Western University London Ontario London Ontario Canada.
² Department of Paediatrics, Pediatric Surgery Western University London Ontario Canada.
³ Department of Pathology and Laboratory Medicine Western University London Ontario Canada.
⁴ Molecular Diagnostics Division London Health Sciences Centre London Ontario Canada.
⁵ Department of Paediatrics, Section of Genetics and Metabolism Western University London Ontario London Ontario Canada.

Abstract

Trisomy 17 is a rare chromosomal disorder. Existing literature on the topic is limited and mostly refer to mosaic Trisomy 17 cases. Our report summarizes the 70-day clinical course of a late preterm neonate with partial Trisomy 17p karyotype 46,XY,der(14)t(14;17)(p11.1;p11.2) dpat. Trisomy 17 due to unbalanced translocation is rare, and our case elaborates the clinical presentation with intestinal malfunction without any anatomical pathology and urethral diverticulum and the ethical dilemma in decision-making. The male proband was born at 35 weeks with antenatal findings of multiple neurological and other abnormalities such as cystic hygroma, absent corpus collosum, high riding third ventricle, absent cavum septum pellucidum, indented occiput, absent ductus venous, and intrauterine growth restriction. The postnatal findings included significant facial dysmorphisms with short palpebral fissures, hypertelorism, low set ears, micrognathia, hirsutism, and single palmar creases, central hypotonia, and hyperreflexia of upper limbs bilaterally. Genital-urinary assessment revealed a urinary diverticulum and significantly underdeveloped scrotum with undescended testes. Infant had excessive irritability and resistance to sleep despite increasing doses of analgesia and sedation, and persistent respiratory and feeding difficulties. Enteral nutrition could not be established due to profuse and persistent diarrhea, necessitating use of total parenteral nutrition. Microarray assay exhibited a pathogenic copy number gain of approximately 21.4 Mb of chromosome region 17p13.3p11.2. Follow-up chromosome analysis and FISH revealed an abnormal male karyotype with a derivative chromosome 14, resulting from an unbalanced translocation between the short arm of one chromosome 14 and the short arm of one chromosome 17, effectively resulting in trisomy 17p11.2. It was derived from a paternal balanced t(14;17)(p11.1;p11.2) as shown by chromosome analysis and FISH studies. The rarity of this chromosomal disorder contributed to difficulty with prognosis and led to bioethical dilemma regarding life-sustaining measures and quality of life. Through shared decision-making processes and in consideration of poor prognosis, parents decided to withdraw life-sustaining care and the proband died at postnatal day of life 70.

Keywords: derivative chromosome 14; partial trisomy 17p; unbalanced translocation.

Publication types

Case Reports