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10.1002/ajmg.c.30323 http://scihub22266oqcxt.onion/10.1002/ajmg.c.30323 C4484722!4484722 !22006661     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=22006661 &cmd=llinks): Failed to open stream: HTTP request failed! 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Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research |pdf=|usr=}}{{22006661 }} gab.com Text Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research JO: Am J Med Genet C Semin Med Genet http://www.kidney.de/pget.php?&tw=1&pmid=22006661 #FOAvip Cyclopia is characterized by the presence of a single eye, with varying degrees of doubling of the intrinsic ocular structures, located in the middle of the face. It is the severest facial expression of the holoprosencephaly (HPE) spectrum. This study describes the prevalence, associated malformations, and maternal characteristics among cases with cyclopia. Data originated in 20 Clearinghouse (ICBDSR) affiliated birth defect surveillance systems, reported according to a single pre-established protocol. A total of 257 infants with cyclopia were identified. Overall prevalence was 1 in 100,000 births (95%CI: 0.89-1.14), with only one program being out of range. Across sites, there was no correlation between cyclopia prevalence and number of births (r = 0.08; P = 0.75) or proportion of elective termination of pregnancy (r = -0.01; P = 0.97). The higher prevalence of cyclopia among older mothers (older than 34) was not statistically significant. The majority of cases were liveborn (122/200; 61%) and females predominated (male/total: 42%). A substantial proportion of cyclopias (31%) were caused by chromosomal anomalies, mainly trisomy 13. Another 31% of the cases of cyclopias were associated with defects not typically related to HPE, with more hydrocephalus, heterotaxia defects, neural tube defects, and preaxial reduction defects than the chromosomal group, suggesting the presence of ciliopathies or other unrecognized syndromes. Cyclopia is a very rare defect without much variability in prevalence by geographic location. The heterogeneous etiology with a high prevalence of chromosomal abnormalities, and female predominance in HPE, were confirmed, but no effect of increased maternal age or association with twinning was observed. Twit Text FOAVip Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research ????Am J Med Genet C Semin Med Genet http://www.kidney.de/pget.php?&tw=1&pmid=22006661 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=22006661 #FOAvip English Wikipedia <ref>{{Cite pmid|22006661 }}</ref> Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research #MMPMID22006661 Orioli IM ; Amar E ; Bakker MK ; Bermejo-Sánchez E ; Bianchi F ; Canfield MA ; Clementi M ; Correa A ; Csáky-Szunyogh M ; Feldkamp ML ; Landau D ; Leoncini E ; Li Z ; Lowry RB ; Mastroiacovo P ; Morgan M ; Mutchinick OM ; Rissmann A ; Ritvanen A ; Scarano G ; Szabova E ; Castilla EE Am J Med Genet C Semin Med Genet 2011[Nov]; 157C (4 ): 344-57 PMID22006661 show ga Cyclopia is characterized by the presence of a single eye, with varying degrees of doubling of the intrinsic ocular structures, located in the middle of the face. It is the severest facial expression of the holoprosencephaly (HPE) spectrum. This study describes the prevalence, associated malformations, and maternal characteristics among cases with cyclopia. Data originated in 20 Clearinghouse (ICBDSR) affiliated birth defect surveillance systems, reported according to a single pre-established protocol. A total of 257 infants with cyclopia were identified. Overall prevalence was 1 in 100,000 births (95%CI: 0.89-1.14), with only one program being out of range. Across sites, there was no correlation between cyclopia prevalence and number of births (r = 0.08; P = 0.75) or proportion of elective termination of pregnancy (r = -0.01; P = 0.97). The higher prevalence of cyclopia among older mothers (older than 34) was not statistically significant. The majority of cases were liveborn (122/200; 61%) and females predominated (male/total: 42%). A substantial proportion of cyclopias (31%) were caused by chromosomal anomalies, mainly trisomy 13. Another 31% of the cases of cyclopias were associated with defects not typically related to HPE, with more hydrocephalus, heterotaxia defects, neural tube defects, and preaxial reduction defects than the chromosomal group, suggesting the presence of ciliopathies or other unrecognized syndromes. Cyclopia is a very rare defect without much variability in prevalence by geographic location. The heterogeneous etiology with a high prevalence of chromosomal abnormalities, and female predominance in HPE, were confirmed, but no effect of increased maternal age or association with twinning was observed. |*International Cooperation [MESH] |Adult [MESH] |Americas/epidemiology [MESH] |Australia/epidemiology [MESH] |Biomedical Research/trends [MESH] |China/epidemiology [MESH] |Chromosome Disorders/genetics [MESH] |Chromosomes, Human, Pair 13/genetics [MESH] |Congenital Abnormalities/*epidemiology/genetics/pathology [MESH] |Epidemiologic Studies [MESH] |Europe/epidemiology [MESH] |Eye Abnormalities/*epidemiology/genetics/pathology [MESH] |Female [MESH] |Holoprosencephaly/epidemiology/genetics/pathology [MESH] |Humans [MESH] |Infant, Newborn [MESH] |Male [MESH] |Population Surveillance/*methods [MESH] |Pregnancy [MESH] |Prevalence [MESH] |Registries [MESH] |Trisomy 13 Syndrome [MESH]Cyclopia: an epidemiologic study in a large dataset from the Internati(epmc).pdf DeepDyve Pubget Overpricing