A 9-year-old girl with phenotypic features of de Grouchy syndrome (deletion 18p)
|Classification and external resources|
Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. The deletion involves the distal section of 18q and typically extends to the tip of the long arm of chromosome 18.
- 1 Nomenclature
- 2 Genetic basis
- 3 Diagnosis
- 4 Clinical description
- 5 Treatment and management
- 6 Current research
- 7 Support resources
- 8 References
Distal 18q- was first described in 1964. Originally, it was called "De Grouchy syndrome" or "De Grouchy syndrome 2". Today, the preferred nomenclature for this condition is 18q-. Since this condition was originally described, researchers have clarified the size and nature of these deletions. In general, deletions of 18q fall into one of two categories: interstitial deletions, which typically have breakpoints between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb), and terminal deletions, which typically have a breakpoint distal to 18q21.1 (45.4 Mb) and extend to the end of the chromosome. If possible, it is preferable to indicate the general location of the deletion with the phrases "proximal 18q-" and "distal 18q-".
Distal 18q- is a deletion of the long arm of chromosome 18. The majority of deletions have breakpoints between 45,405,887 and the tip of the chromosome. There are no common breakpoints, thus the size of the deletions vary widely. The largest deletion reported is 30.076 Mb, while the smallest deletion reported to cause a clinical phenotype is 3.78 Mb.
Suspicion of a chromosome abnormality is typically raised due to the presence of developmental delays or birth defects. Diagnosis of distal 18q- is usually made from a blood sample. A routine chromosome analysis, or karyotype, is usually used to make the initial diagnosis, although it may also be made by microarray analysis. Increasingly, microarray analysis is also being used to clarify breakpoints. Prenatal diagnosis is possible using amniocentesis or chorionic villus sampling.
Distal 18q- causes a wide range of medical and developmental concerns, with significant variation in severity due to the variation in breakpoints reported in individuals with distal 18q-. Current research is focused on establishing genotype-phenotype correlations to enable predictive genotyping.
Heart abnormalities are present in 25–35% of people with distal 18q-. The majority of these defects are septal. Congenital orthopedic anomalies are also relatively common, particularly rocker-bottom feet or clubfoot. Cleft lip and palate are relatively common in people with distal 18q-. Kidney abnormalities have also been reported and include horseshoe kidney, hydronephrosis, polycystic kidney, and absent kidney. Boys with distal 18q- may have genital anomalies, the most frequent being cryptorchidism and hypospadias.
Ear and sinus infections
Due to changes in facial structures, infants, toddlers, and children with distal 18q- often have poor drainage from the middle ears, leading to a build-up of fluid. This can in turn lead to recurrent ear and sinus infections. Antibiotics are typically required to treat these infections. In addition, the diagnosis of ear infections in children with 18q- is frequently complicated by stenosis or atresia of the ear canals, a common finding in people with distal 18q-.
People with distal 18q- frequently have conductive and/or sensorineural hearing loss. The degree of hearing loss may vary from a mild to a severe loss.
As mentioned above, males with distal 18q- may have cryptorchidism. Hypospadias and chordee have also been reported. Also, a variety of kidney malformations have been reported in infants with distal 18q-, as noted above. Additionally, vesicouretereral reflux has been diagnosed in several people with distal 18q-.
As mentioned above, distal 18q- is associated with an increased incidence of clubfoot and rocker bottom feet. Also, a significant chance of developing pes planus or pes cavus exists. People with distal 18q- frequently have overlapping toes. Scoliosis and genu varum are also known orthopedic complications in children and adults with distal 18q-.
Children and adults with distal 18q- are often small for their age. Many people with distal 18q- have an abnormal response to growth hormone stimulation. Those who have been treated with growth hormone have responded well to the treatment. Microcephaly is also common in people with distal 18q-.
Hypothyroidism has been reported in some people with distal 18q-.
Several people with distal 18q- have been diagnosed with low IgA levels, resulting in an increased incidence of infections.
An increased incidence of psychiatric conditions occurs within the distal 18q- population. In one study, nearly 60% had depressive symptoms, 60% had symptoms of an anxiety disorder, 25% had manic symptoms, and 25% had psychotic symptoms. However, this study included young patients, many of whom were too young to exhibit signs of certain psychiatric conditions. The typical age of onset for many of these conditions appears to be during the teen years. Thus, the results of this study may actually underestimate the true incidence of psychiatric conditions within this population.
Cognition and adaptive skills
The intellectual development of individuals with distal 18q- vary quite widely. In one study of 46 individuals with distal 18q-, IQ ranged from 49 to 113, with most individuals falling in the mild to moderate range of intellectual disability. Some of those with IQ scores on the lower end of the spectrum probably actually had deletions encompassing the TCF4 gene.
An increased incidence of autism is seen within the distal 18q- population. In a recent study, 45 of 105 individuals evaluated fell into the "possible" or "very likely" levels of risk for autism. Adaptive skills may also be delayed in people with distal 18q-.
Common facial features include midfacial hypoplasia, short and downward- or upward-slanting palpebral fissures, epicanthic folds, and low-set ears with a prominent antihelix.
Treatment and management
At present, treatment for distal 18q- is symptomatic, meaning the focus is on treating the signs and symptoms of the conditions as they arise. To ensure early diagnosis and treatment, people with distal 18q- are suggested to undergo routine screenings for thyroid, hearing, and vision problems.
Currently, research is focusing on identifying the role of the genes on 18q in causing the signs and symptoms associated with distal deletions of 18q.
TCF4 – In 2007, deletions of or point mutations in this gene were identified as the cause of Pitt-Hopkins syndrome. This is the first gene that has been definitively shown to directly cause a clinical phenotype when deleted. If a deletion includes the TCF4 gene (located at 52,889,562-52,946,887), features of Pitt-Hopkins may be present, including abnormal corpus callosum, short neck, small penis, accessory and wide-spaced nipples, broad or clubbed fingers, and sacral dimple. Those with deletions inclusive of TCF4 have a significantly more severe cognitive phenotype.
Critical regions – Recent research has narrowed the critical regions for four features of the distal 18q- phenotype down to a small segment of distal 18q, although the precise genes responsible for those features remain to be identified.
The table below shows the established critical regions for four features of distal 18q-, as well as the penetrance for each of those features. The penetrance figure represents the likelihood a person would have the feature given the critical region is deleted.
|Feature||Critical Region||Chromosome Bands||Penetrance|
|Growth hormone response failure||71,669,548-73,287,604||18q22.3-q23||90%|
Haplolethal regions - Two regions on chromosome 18 have never been found to be deleted. They are located between the centromere and 22,826,284 bp (18q11.2) and between 43,832,732 and 45,297,446 bp (18q21.1). The genes in these regions are thought to be lethal when deleted.
- De Grouchy J, Royer P, Salmon C, Lamy M (1964). "Deletion partielle du bras longs du chromosome 18". Path Biol (Paris) 12: 579–582.
- Heard PL, Carter EM, Crandall AC, Sebold C, Hale DE, Cody JD (July 2009). "High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH)". Am. J. Med. Genet. A 149A (7): 1431–7. doi:10.1002/ajmg.a.32900. PMC 2731576. PMID 19533772.
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- Lancaster JL, Cody JD, Andrews T, Hardies LJ, Hale DE, Fox PT (March 2005). "Myelination in children with partial deletions of chromosome 18q". AJNR Am J Neuroradiol 26 (3): 447–54. PMID 15760848.
- Kochunov P, Lancaster J, Hardies J, et al. (April 2005). "Mapping structural differences of the corpus callosum in individuals with 18q deletions using targetless regional spatial normalization". Hum Brain Mapp 24 (4): 325–31. doi:10.1002/hbm.20090. PMID 15704090.
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- Zavala J, Ramirez M, Medina R, et al. (April 2010). "Psychiatric syndromes in individuals with chromosome 18 abnormalities". Am. J. Med. Genet. B Neuropsychiatr. Genet. 153B (3): 837–45. doi:10.1002/ajmg.b.31047. PMID 19927307.
- Semrud-Clikeman M, Thompson NM, Schaub BL, et al. (September 2005). "Cognitive ability predicts degree of genetic abnormality in participants with 18q deletions". J Int Neuropsychol Soc 11 (5): 584–90. doi:10.1017/S1355617705050691. PMID 16212685.
- O'Donnell L, Soileau B, Heard P, et al. (August 2010). "Genetic determinants of autism in individuals with deletions of 18q". Hum. Genet. 128 (2): 155–64. doi:10.1007/s00439-010-0839-y. PMID 20499253.
- Zweier C, Peippo MM, Hoyer J, et al. (May 2007). "Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome)". Am. J. Hum. Genet. 80 (5): 994–1001. doi:10.1086/515583. PMC 1852727. PMID 17436255.
- Feenstra et al. (2011). "Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humans". Am J Hum Genet 89 (6): 813–9. doi:10.1016/j.ajhg.2011.11.008. PMC 3234381. PMID 22152683.
- Cody JD, Heard PL, Crandall AC, et al. (July 2009). "Narrowing critical regions and determining penetrance for selected 18q- phenotypes". Am. J. Med. Genet. A 149A (7): 1421–30. doi:10.1002/ajmg.a.32899. PMID 19533771.