- Case report
- Open Access
Clinical utility of chromosomal microarray analysis in the diagnosis and management of monosomy 7 mosaicism
© Dwivedi et al.; licensee BioMed Central Ltd. 2014
Received: 18 September 2014
Accepted: 25 November 2014
Published: 4 December 2014
There have been dramatic improvements in our ability to more accurately diagnose the underlying genetic causes of developmental delay/intellectual disability; however, there is less known about the treatment trajectory and whether or not patient management and outcomes have changed due to the information gained from genetic testing. Here we report a case study of a 20-month-old male first referred to the genetics clinic in 2008 for interhemispheric cysts, agenesis of the corpus callosum, left cortical dysplasia, and developmental delay of unknown etiology. The diagnostic work-up for this patient included chromosomal microarray which detected >20% mosaicism for monosomy 7, which raised concern for a possible myelodysplastic syndrome. The clone was not detected in stimulated peripheral blood cultures and his karyotype was reported as a normal male. Because of this microarray finding, he was referred to pediatric hematology/oncology where he was confirmed to have a pre-symptomatic diagnosis of myelodysplastic syndrome and was treated with chemotherapy and a bone-marrow transplant. This case illustrates the clinical utility of microarray testing and the importance of long-term follow-up to assess patient outcomes.
Over the past ten years, a dramatic shift in clinical laboratory testing has taken place in the assessment of patients with suspected genetic abnormalities related to developmental delay/intellectual disability, congenital anomalies, and dysmorphic features from low resolution techniques to high resolution genomic technologies.
Traditionally, karyotyping and fluorescence in situ hybridization (FISH) were the methods used for cytogenetic analysis. Karyotyping can detect aberrations at a resolution averaging 5–10 megabases while FISH, a more sensitive technique, enables visualization of targeted chromosomal regions at a resolution of greater than or equal to 150 kilobases. However, FISH is limited in its application by the probes used to detect a specific genetic locus. For this reason, karyotyping and FISH have been commonly used in tandem in clinical practice (karyotyping to visualize the whole genome and FISH to target specific locations at a higher resolution) in order to improve diagnostic yield.
Over the past decade, microarray technology has transitioned from the research laboratory to the clinical laboratory and is used for assessing copy number variations (CNVs) in patients undergoing diagnostic testing for developmental delay/intellectual disability due to its ability to assess DNA copy number across the entire genome at a resolution not possible with karyotype or FISH . Furthermore, the American College of Medical Genetics and Genomics (ACMG) Practice Guidelines published in 2011 and revised in 2013 recommend that genomic microarrays be used as first-tier tests for the postnatal evaluation of individuals with developmental delay/intellectual disability ,. However, current laboratory practices for chromosomal testing vary and can range from a microarray as the sole diagnostic test of choice, to a combination of several methods (e.g. microarray, karyotype, FISH, and Fragile X testing by polymerase chain reaction based methods) ,.
There are many reports in the scientific literature about the increase in diagnostic yield by employing microarray technology . However, there is less information about how this improved diagnostic yield translates into better clinical outcomes. The current case serves as an example of this enhanced patient outcome made possible by chromosomal microarray. Secondly, this also highlights that improvements in diagnostic yield are not limited only to increased resolution but also allow for the detection of chromosome abnormalities in non-dividing cells.
A prenatal ultrasound at 22 weeks gestation revealed agenesis of the corpus callosum, suspected interhemispheric cysts, and cortical dysplasia for the male patient. There were no other complications or exposures during the pregnancy. The delivery was normal. The birth weight was 3,976 grams (75-90th percentile), the birth length was 53.5 cm (75-90th percentile), and the birth head circumference was 36.5 cm (75-90th percentile). He was noted to be irritable at birth, but was otherwise well. The child’s parents are both healthy. The mother previously had a miscarriage at 12 weeks. The child has 1 healthy brother.
The patient had a number of normal abdominal ultrasounds. He had chronic ear infections and received PE tubes at 16 months old. Developmentally, the patient sat at 6–7 months and walked at 19 months. He was referred to speech therapy due to concerns about speech delay.
Materials and methods
Chromosome analysis revealed a normal, 46,XY karyotype. Initially, neither microarray nor MLPA subtelomere analysis could be performed on the original blood samples (taken at birth) due to DNA degradation.
Monosomy 7 mosaicism has been causally linked to gain of function mutations in RAS pathway genes . As a result, clinical sequencing of the RAS pathway genes PTPN11, SOS1, RAF1, and KRAS was completed and all results were normal.
Monosomy 7 mosaicism was not felt to be the explanation for the patient’s clinical features; however, due to reports of an association between monosomy 7 mosaicism and myelodysplasia, the patient was referred to a pediatric hematologist/oncologist for further evaluation. The patient had a bone marrow biopsy which revealed evidence of myelodysplasia. He subsequently had chemotherapy and a bone marrow transplant at 4 years old.
Almost one year after surgery, he was seen at the genetics clinic for a follow-up visit. It was noted that several follow-up bone marrow biopsies indicated normal bone marrow without evidence of myelodysplasia. Chromosome analysis and FISH for monosomy 7 were normal following the bone marrow transplant. The patient was doing well with no subsequent issues and was not taking any medications. He had a number of dental cavities attributed to the use of chemotherapy but was making developmental progress. He had decreased use of his right hand and right leg and preferred to use his left hand.
Monosomy 7 is one of the most frequent chromosomal abnormalities observed in myelodysplasia and acute myelogenous leukemia (AML) ,. Other congenital bone marrow disorders, such as Fanconi anemia, congenital neutropenia and familial monosomy 7, predispose to leukemia usually through a myelodysplastic phase ,-. Early detection and identification of monosomy 7 by microarray may allow for earlier diagnosis and intervention which may translate into improved patient prognosis.
We report the detection of monosomy 7 mosaicism in a child referred for genetic testing due to mild developmental delay, agenesis of the corpus callosum, interhemispheric cysts, and left cortical dysplasia. The percent mosaicism for monosomy 7 was readily detected and quantified by microarray and FISH analysis but not by high resolution chromosome analysis.
Monosomy 7 mosaicism was not felt to be the explanation for his presenting clinical features. Neither did he have symptoms, such as easy bruising or petechiae that would suggest an underlying diagnosis of myelodysplasia. Due to the association of monosomy 7 mosaicism with myelodysplasia, he was referred to hematology/oncology and confirmed to have myelodysplasia based on bone marrow biopsy. He subsequently had a bone marrow transplant with apparently curative outcome.
Monosomy 7 is considered a poor prognostic sign in individuals with myelodysplasia . However, the early detection of monosomy 7 prior to the development of any related hematologic symptoms is believed to have improved our patient’s long-term prognosis. If microarray had not detected monosomy 7 mosaicism during his evaluation for other unrelated clinical features, the diagnosis of myelodysplasia and subsequent bone marrow transplant would likely have been significantly delayed, resulting in a worse prognosis for our patient. Given the lack of correlation of the level of mosaicism and myelodysplaisa, any level of mosaicism for monosomy 7 would warrant further hematological evaluation for possible myelodysplasia.
In conclusion, we believe that the fortuitous identification of monosomy 7 mosaicism by microarray significantly improved the clinical outcome for our patient. The microarray result led to a referral to hematology/oncology which would not have otherwise happened until he developed symptoms of a hematologic disorder. This demonstrates the benefits of multi-disciplinary collaboration when a significant microarray result is identified as having a potential impact on the management of a patient.
We would like to thank the family for their participation and written informed consent was obtained for the publication of this case report and any accompanying images. We also thank Dr. Michelle Hudspeth for the care provided and follow-up clinical reports after identification of myelodysplasia in the patient.
- Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, et al.: Consensus statement: Chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 2010,86(5):749–764. 10.1016/j.ajhg.2010.04.006PubMed CentralView ArticlePubMedGoogle Scholar
- Kearney HM, Thorland EC, Brown KK, Quintero-Rivera F, South ST; Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee: American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants Genet Med 2011,13(7):680–685. 10.1097/GIM.0b013e3182217a3aView ArticleGoogle Scholar
- South ST, Lee C, Lamb AN, Higgins AW, Kearney HM: Working Group for the American College of Medical Genetics and Genomics Laboratory Quality Assurance Committee: ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013. Genet Med 2013,15(11):901–909. 10.1038/gim.2013.129View ArticlePubMedGoogle Scholar
- Michelson DJ, Shevell MI, Sherr EH, Moeschler JB, Gropman AL, Ashwal S: Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology 2011,77(17):1629–1635. 10.1212/WNL.0b013e3182345896View ArticlePubMedGoogle Scholar
- Moeschler JB: Genetic evaluation of intellectual disabilities. Semin Pediatr Neurol 2008,15(1):2–9. 10.1016/j.spen.2008.01.002View ArticlePubMedGoogle Scholar
- McNerney ME, Brown CD, Peterson AL, Banerjee M, Larson RA, Anastasi J, LeBeau MM, White KP: The spectrum of somatic mutations in high-risk acute myeloid leukaemia with −7/del(7q). Br J Haematol 2014,166(4):550–556. 10.1111/bjh.12964View ArticlePubMedGoogle Scholar
- Aktas D, Tuncbilek E: Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study. Cancer Genet Cytogenet 2006,171(1):72–75. 10.1016/j.cancergencyto.2006.06.010View ArticlePubMedGoogle Scholar
- Gaitonde S, Boumendjel R, Angeles R, Rondelli D: Familial childhood monosomy 7 and associated myelodysplasia. J Pediatr Hematol Oncol 2010,32(6):e236-e237. 10.1097/MPH.0b013e3181e75759View ArticlePubMedGoogle Scholar
- Hasle H, Niemeyer CM: Advances in the prognostication and management of advanced MDS in children. Br J Haematol 2011,154(2):185–195. 10.1111/j.1365-2141.2011.08724.xView ArticlePubMedGoogle Scholar
- Pasquet M, Bellanné-Chantelot C, Tavitian S, Prade N, Beaupain B, Larochelle O, Petit A, Rohrlich P, Ferrand C, Van Den Neste E, Poirel HA, Lamy T, Ouachée-Chardin M, Mansat-De Mas V, Corre J, Récher C, Plat G, Bachelerie F, Donadieu J, Delabesse E: High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. Blood 2013,121(5):822–829. 10.1182/blood-2012-08-447367PubMed CentralView ArticlePubMedGoogle Scholar
- Thurston VC: Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literature. Cancer Genet Cytogenet 1999,109(2):154–160. 10.1016/S0165-4608(98)00167-8View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.