Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome

被引:7
作者
Schoen, Michael [1 ]
Lapunzina, Pablo [2 ,3 ,4 ]
Mattina, Teresa [2 ,3 ,4 ,5 ]
Gunnarsson, Cecilia [6 ,7 ]
Hadzsiev, Kinga [8 ]
Verpelli, Chiara [9 ]
Bourgeron, Thomas [10 ]
Jesse, Sarah [11 ]
Van Ravenswaaij-Arts, Conny M. A. [12 ]
Hennekam, Raoul C. [12 ]
机构
[1] Ulm Univ, Inst Anat & Cell Biol, Ulm, Germany
[2] Hosp Univ La Paz, Inst Genet Med & Mol INGEMM IdiPAZ, Madrid, Spain
[3] ISCIII, Ctr Invest Biomed en Red Enfermedades Raras, CIBERER, Madrid, Spain
[4] Hosp La Paz, ITHACA, European Reference Network, Madrid, Spain
[5] Univ Catania, Dept Biomed & Biotechnol Sci, Med Genet, Catania, Italy
[6] Linkoping Univ, Ctr Rare Dis South East Reg Sweden, Dept Clin Genet, Linkoping, Sweden
[7] Linkoping Univ, Ctr Rare Dis South East Reg Sweden, Dept Biomed & Clin Sci, Linkoping, Sweden
[8] Univ Pecs, Med Sch, Dept Med Genet, Pecs, Hungary
[9] CNR Neurosci Inst, Milan, Italy
[10] Univ Paris Cite, Inst Pasteur, Genet Humaine & Fonct Cognit, UMR3571 CNRS ,IUF, Paris, France
[11] Ulm Univ, Dept Neurol, Ulm, Germany
[12] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[13] Univ Amsterdam, Med Ctr, Dept Pediat, Amsterdam, Netherlands
基金
欧盟地平线“2020”;
关键词
Phelan-McDermid syndrome; PMS; 22q13 deletion syndrome; SHANK3; Genotype-phenotype correlation; Natural history; Clinical trials; INTERSTITIAL; 22Q13; DELETIONS; MOLECULAR CHARACTERIZATION; SHANK3; AUTISM; REARRANGEMENTS; EXPRESSION; SPECTRUM; GENES; HAPLOINSUFFICIENCY; MUTATIONS;
D O I
10.1016/j.ejmg.2023.104754
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Phelan-McDermid syndrome (PMS) is an infrequently described syndrome that presents with a disturbed development, neurological and psychiatric characteristics, and sometimes other comorbidities. As part of the development of European medical guidelines we studied the definition, phenotype, genotype-phenotype characteristics, and natural history of the syndrome. The number of confirmed diagnoses of PMS in different European countries was also assessed and it could be concluded that PMS is underdiagnosed. The incidence of PMS in European countries is estimated to be at least 1 in 30,000. Next generation sequencing, including analysis of copy number variations, as first tier in diagnostics of individuals with intellectual disability will likely yield a larger number of individuals with PMS than presently known. A definition of PMS by its phenotype is at the present not possible, and therefore PMS-SHANK3 related is defined by the presence of SHANK3 haploinsufficiency, either by a deletion involving region 22q13.2-33 or a pathogenic/likely pathogenic variant in SHANK3. In summarizing the phenotype, we subdivided it into that of individuals with a 22q13 deletion and that of those with a pathogenic/likely pathogenic SHANK3 variant. The phenotype of individuals with PMS is variable, depending in part on the deletion size or whether only a variant of SHANK3 is present. The core phenotype in the domains development, neurology, and senses are similar in those with deletions and SHANK3 variants, but individuals with a SHANK3 variant more often are reported to have behavioural disorders and less often urogenital malformations and lymphedema. The behavioural disorders may, however, be a less outstanding feature in individuals with deletions accompanied by more severe intellectual disability. Data available on the natural history are limited. Results of clinical trials using IGF-1, intranasal insulin, and oxytocin are available, other trials are in progress. The present guidelines for PMS aim at offering tools to caregivers and families to provide optimal care to individuals with PMS.
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