Article
[4p trisomy secondary to paternal translocation t(4p-;15q+)].
Annales de pediatrie - 1 May 1991
Saad A, Khelif M, Kharrat H, Bouzakoura C
Abstract excerpt
A new case of trisomy 4p is reported. The patient was a boy with dysmorphism, growth failure and developmental retardation. Craniofacial features included microcephaly with a flat forehead, a prominent glabella, hyperteleorism, a broad, concave nasal bridge, a bulb-shaped nose, a wide mouth with...
Topics
- Child, Preschool
- Chromosomes, Human, Pair 4
- Fathers
- Humans
- Karyotyping
- Male
- Phenotype
- Translocation, Genetic
- Trisomy
