Related Experiment Video
Updated: Jun 10, 2026

Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome
Published on: October 3, 2018
Familial childhood monosomy 7 and associated myelodysplasia
Sujata Gaitonde1, Redouane Boumendjel, Ronald Angeles
1Department of Pathology, University of Illinois, College of Medicine, Chicago 60612, USA. sgaitond@uic.edu
Insights
Familial monosomy 7, a rare genetic condition, affects siblings with bone marrow abnormalities and often presents with neurological or blood disorders in childhood. This report details the 14th identified family with this condition.
Area of Science:
- Genetics
- Hematology
- Pediatrics
Background:
- Familial monosomy 7 is a rare cytogenetic abnormality.
- It is characterized by bone marrow monosomy 7 in multiple siblings.
- This condition typically manifests in childhood with associated neurological and/or hematologic disorders.
Summary:
Familial monosomy 7 is defined as bone marrow monosomy 7 occurring as a sole cytogenetic abnormality affecting 2 or more siblings. It manifests usually in childhood with neurologic disorder (cerebellar ataxia or atrophy) and/or hematologic disorder (marrow hypoplasia, myelodysplasia, acute myeloid leukemia, or pancytopenia). Partial or complete monosomy 7 with hematologic disorder has been reported in 13 families/pedigrees to date. Here we report the 14th family.
Related Concept Videos
Genomic Imprinting and Inheritance
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
Meiosis I
Nondisjunction
Nondisjunction
Differentiation of Common Myeloid Progenitor Cells
Abnormal Proliferation

