Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes
- PMID: 9894164
Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes
Abstract
We present genotype-phenotype correlations in two patients with distal 10q deletion. A patient with a small terminal deletion presented mild mental retardation and behavioral difficulties with hyperactivity, whereas the patient with a larger deletion, had multiple congenital anomalies and moderate mental retardation. Our observation confirms the previous suggestion that larger deletions of distal chromosome 10q are associated with a more severe clinical presentation, whereas hyperactive behavior may be a specific feature of small terminal deletions of chromosome 10q26.
Similar articles
-
Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.Am J Med Genet. 1988 Nov;31(3):533-48. doi: 10.1002/ajmg.1320310308. Am J Med Genet. 1988. PMID: 3067575 Review.
-
A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?Genet Couns. 1996;7(1):53-9. Genet Couns. 1996. PMID: 8652089 Review.
-
A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.Am J Med Genet. 1990 Dec;37(4):471-4. doi: 10.1002/ajmg.1320370409. Am J Med Genet. 1990. PMID: 2260590 Review.
-
A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.Genet Couns. 2008;19(4):365-71. Genet Couns. 2008. PMID: 19239079
-
Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.Genet Couns. 2005;16(2):129-38. Genet Couns. 2005. PMID: 16080292
Cited by
-
An interstitial deletion at 10q26.2q26.3.Case Rep Genet. 2014;2014:505832. doi: 10.1155/2014/505832. Epub 2014 Feb 6. Case Rep Genet. 2014. PMID: 24649379 Free PMC article.
-
Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease.Front Genet. 2017 Oct 9;8:143. doi: 10.3389/fgene.2017.00143. eCollection 2017. Front Genet. 2017. PMID: 29062322 Free PMC article.