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Updated: Aug 15, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
Skeletal dysplasia in an infant with hypertelorism, hypospadias, developmental delay, and a complex chromosomal
Insights
A male infant presented with hypertelorism, hypospadias, and skeletal dysplasia. Chromosomal abnormalities and other congenital issues suggest either a variant of BBB syndrome or a novel genetic disorder.
Area of Science:
- Medical Genetics
- Clinical Dysmorphology
- Pediatric Endocrinology
Background:
- Hypertelorism and hypospadias are congenital anomalies with diverse etiologies.
- Metaphyseal dysplasia indicates a group of skeletal disorders affecting bone growth.
- Congenital nystagmus and hearing impairment can be associated with various genetic syndromes.
Abstract:
A male infant with hypertelorism and hypospadias was found to have skeletal changes suggesting metaphyseal dysplasia. Associated findings included congenital nystagmus, hearing impairment, and a complex translocation involving the number 5, 8, and 10 chromosomes. Although some of these abnormalities may be coincidental, they might represent infrequent components of the BBB syndrome. It is just as likely, however, that the syndrome is a new one.
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