Distal 11q monosomy syndrome: a report of two Egyptian sibs with normal parental karyotypes confirmed by molecular cytogenetics

• Published in: Genetic counseling Vol. 19; no. 1; p. 47
• Main Authors: Afifi, H H, Zaki, M S, El-Gerzawy, A M S, Kayed, H F
• Format: Journal Article
• Language: English
• Published: Switzerland 2008
• Subjects: Atrophy - pathology; Child; Child, Preschool; Chromosomes, Human, Pair 11 - genetics; Coloboma; Cytogenetics - methods; Egypt; Female; Humans; In Situ Hybridization, Fluorescence; Jacobsen Distal 11q Deletion Syndrome - genetics; Karyotyping; Male; Monosomy - genetics; Optic Nerve - pathology; Parents; Pedigree; Psychomotor Disorders; Siblings; Strabismus; Egypt
• ISSN: 1015-8146

Jacobsen syndrome is a rare disorder, caused by segmental monosomy for the distal end of the long arm of chromosome 11 with variable phenotypic expressivity. We report on the first male (6 years old) and female (3 years old) sibs with clinical and cytogenetics characterization of Jacobsen syndrome. Their karyotypes showed deletion 11q23.3-qter. Patients presented with growth and psychomotor retardation, facial dysmorphism, eye anomalies, and congenital heart disease (variable degrees of septal defect). Family history revealed a clinically similar brother, who died at 2 months old from cardiac anomalies in the form of single ventricle without being subjected to further investigations. Chromosomal analysis of the parents was normal. Karyotyping for the 2 patients and their parents was confirmed by fluorescence in situ hybridization analysis (FISH) using whole chromosome painting probes for 11 (WCP 11). Relevant investigations for both sibs showed mild thrombocytopenia with normal platelets morphology and striking periventricular demyelination on neuroimaging. Inguinal small testicles as well as focal epileptiform dysfunction were recorded in the male patient only. Abdominal ultrasound, hearing test, and DEXA scan were normal in both patients. Due to of the presence of apparently 3 affected offspring and normal parental karyotypes, an inherited predisposition was highly suspected. The large size of the distal deleted 11q segment in our patients support the recent hypothesis, that Jacobsen syndrome is a chromosomal deletion syndrome with genetic predisposition, due to expansion of p(CCG)n trinucleotide in the folate-sensitive fragile site FRA11B, at breakpoint 11q23.3. In conclusion, identification and further delineation of more similar patients will contribute to understanding the genetic basis of the 11q phenotype.