Handbook of Genetic Counseling/Cri-du-chat syndrome - deletion 5p

Cri-du-chat syndrome - deletion 5p Contracting Introduction Ask about what their main concerns are Explain that we will update medical and developmental history since her last visit to genetics Doctor will perform physical examination We will discuss your concerns and any recommendations we have Interim History (Follow form, but specifically ask about list of potential health problems located below Overview) Cri du chat is a syndrome that is associated with a deletion of the short arm of chromosome 5 French for "cat's cry" incidence is 1:50,000 (Van Buggenout et al., 2000 ) may be as high as 1:20,000 (OMIM) Characteristic features usually suspected at birth based on characteristic monochromatic, high-pitched cry poor suck, vomiting, failure to thrive, respiratory distress and jaundice present in 60-92% microcephaly round face hypertelorism epicanthal folds down-slanting palpebral fissures low-set ears micrognathia psychomotor retardation high arched palate as individuals with 5p deletion get older change of phenotype is noted and it is less striking and harder to diagnose (face lengthens, face becomes "coarse", prominent supra-orbital ridges, deep-set eyes, hypoplastic nasal bridge, severe dental malocclusion, relatively large mouth, and full lower lip) Potential health problems several cardiac anomalies described in a small number of patients (ASD, VSD, tetralogy of fallot and PDA) cleft palate (rare) gastrointestinal abnormalities include malrotation and Hirschprung disease teeth abnormally erupted Apnea Strabismus Minor vision problems Gastric reflux Chronic constipation (well managed in most cases) Colic Frequent ear and upper respiratory infections Scoliosis Sleep disorders Saliva control problems (if not resolved during childhood surgery can help correct) Minor hearing impairment Growth compared with the standard population, most children with cri-du-chat syndrome are small at birth as they grow most have significant microcephaly weight compromised for age slow growth frequently observed may be evidence of intrauterine growth retardation Life expectancy Difficult to predict 10% mortality in first year due to respiratory or cardiac complications Believed that if no major health problems present life span would be in normal range Learning study of 26 children ages 6 yr. 4 mths and 15 yr 5 mths moderate to severe learning difficulties and developmental delay are usually observed 24 were in severe learning disability range better receptive than expressive language study of seven patients 6 severe or profound MR 1 mild MR Language comprehension may not be as impaired as language production Clear benefit shown in those children that received early intervention services compared to those that did not Developed many self-care skills Communicate through short sentences, words, signs, or gestures Behavior study examined the range, distinctiveness, and correlates of maladaptive behavior in 146 subjects using the Aberrant *Behavior Checklist as a standardized measure Hyperactivity was the most significant and frequent problem in the sample Subjects also showed aggression, tantrums, self-injurious behavior some of these problems were more pronounced in individuals with lower cognitive-adaptive levels, as well as in those with histories of previous medication trials Autistic-like features and social withdrawal were more characteristic of individuals with translocations as opposed to deletions, even when controlling for the lower adaptive level of the translocation group head banging, hitting the head against body parts, self-biting and rumination are the most frequently occurring behaviours in CCS Aggressive behaviour was reported for 88%, with a statistically significant negative correlation between age and the number of aggressive behaviors reported Study of 7 older patients most had periods of destructive behavior, self mutilation and aggression Other reported behaviors include: Repetitive movements Obsessive attachment to objects Hypersensitivity to sensory stimuli Feeding and sleeping problems Mood disorders Genetics 85% are sporadic deletions *10-15% are familial (usually parental translocation rarely a familial inversion) PARENTAL CHROMOSOMES SHOULD BE DONE SO ACCURATE RECURRANCE RISKS CAN BE CALCULATED Gene that makes Delta-catenin (an adherends junction protein involved in cell motility and expressed early in neuronal development) delta-catenin maps to a specific region in 5p15.2 that has been implicated in the mental retardation phenotype strong correlation between the hemizygous loss of delta-catenin and severe mental retardation Genotype-phenotype correlation Patients show phenotypic and cytogenetic variability Genotype-phenotype correlation in 62 patients with terminal deletions highlighted a progressive severity of clinical manifestation and psychomotor retardation related to the size of the deletion (Mainardi et al., 2001). Whereas other study reported no correlation with size of deletion and severity in 50 patients (Marinescu et al., 1999). The analysis of seven patients with interstitial deletions and one with a small terminal deletion confirmed the existence of two critical regions, one for dysmorphism and mental retardation in p15.2 and the other for the cat cry in p15.3 study lends support to the hypothesis of a separate region in p15.3 for the speech delay One family with deletion 5p where breaking point is slightly distal to 15.3 showed only Patient resources/ references 5p- Society (Cri-du-Chat) -- support group 11609 Oakmont Overland Park, KS 66210 Phone: (913) 469-8900 E-mail: fivepminus@aol.com Web Site: http://www.fivepminus.org/ Conference in SLC Aug 15-19, 2002 Chromosome Deletion Outreach P.O. Box 724 Boca Raton, FL 33429-0724 E-mail: cdo@worldnet.att.net Web site:members.aol.com/cdousa/cdo.htm Cri Du Chat Support Group of Australia Inc. Email: info@criduchat.asn.au <mailto:info@criduchat.asn.au> Web: http://www.criduchat.asn.au References Mainardi, P C; Perfumo, C; Cali, A; Coucourde, G; Pastore, G; Cavani, S; Zara, F; Overhauser, J; Pierluigi, M; Bricarelli, F D. Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation. JOURNAL OF MEDICAL GENETICS. vol. 38, no. 3 (2001 Mar): 151-8. Collins, M S Ross; Cornish, K. A survey of the prevalence of stereotypy, self-injury and aggression in children and young adults with Cri du Chat syndrome. JOURNAL OF INTELLECTUAL DISABILITY RESEARCH. vol. 46, no. Pt 2 (2002 Feb): 133-40. Medina, M; Marinescu, R C; Overhauser, J; Kosik, K S. Hemizygosity of delta-catenin (CTNND2) is associated with severe mental retardation in cri-du-chat syndrome. GENOMICS. vol. 63, no. 2 (2000 Jan 15): 157-64. Cornish, K M; Cross, G; Green, A; Willatt, L; Bradshaw, J M. A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis. JOURNAL OF MEDICAL GENETICS. vol. 36, no. 7 (1999 Jul): 567-70. Marinescu, RC, et al. No relationship between the size of the deletion and level of developmental delay in cri-du-chat syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS. vol. 86, no. 1 (1999 Sep 3): 66-70. Cornish, K M; Bramble, D; Munir, F; Pigram, J. Cognitive functioning in children with typical cri du chat (5p-) syndrome. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY. vol. 41, no. 4 (1999 Apr): 263-6. Van Buggenhout, G.J.C.M. et al. Cri du Chat Syndrome: Changing Phenotype in Older Patients. AMERICAN JOURNAL OF MEDICAL GENETICS. 90:203-215 (2000). Notes The information in this outline was last updated in 2002.