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1,120 Possible Causes for Agenesis of Corpus Callosum, Failure to Thrive, Multiple Congenital Anomalies

  • Fetal Warfarin Syndrome

    […] to thrive Numerology Chaldean Numerology The numerical value of fetal warfarin syndrome in Chaldean Numerology is: 6 Pythagorean Numerology The numerical value of fetal warfarin[] The congenital abnormalities include nasal bridge depression, nasal bones hypoplasia, microcephaly, congenital heart disorders, and brachydactyly.[] […] of corpus callosum microcephaly microphthalmia congenital cataracts cardiovascular congenital cardiac anomalies Warfarin is a teratogenic drug.[]

  • Wolf-Hirschhorn Syndrome

    Accordingly, prenatal-onset growth retardation and failure to thrive have been found to result from haploinsufficiency for a 4p gene located between 0.4 and 1.3 Mb, whereas[] […] of the corpus callosum, bilateral renal hypoplasia, and two atrial septal defects.[] The present case shows that not only deletions but also duplications of the Wolf-Hirshhorn critical region cause mental retardation and multiple congenital anomalies.[]

  • Lenz-Majewski Syndrome

    The disorder is characterized by failure to thrive and mental retardation.[] […] of corpus callosum 0001274 Bifid uvula 0000193 External genital hypoplasia Underdevelopment of external reproductive organs 0003241 High, narrow palate Narrow, high-arched[] congenital anomalies, mental retardation and progressive skeletal sclerosis Statements Identifiers Sitelinks Wikipedia (3 entries) edit Wikibooks (0 entries) edit Wikiquote[]

  • Patau Syndrome

    Infants who survive to one year have severe complications including intellectual disability, seizures and failure to thrive.[] . * Agenesis of the Corpus Callosum * Enlarged Cisterna Magna. * Microcephaly. * Meningocele / encephalocele.[] Trisomy 13 or Patau syndrome (PS) is a chromosomal disorder characterized by a well known presentation of multiple congenital anomalies.[]

  • Mowat-Wilson Syndrome

    Symptons may include: Growth and Motor development delay : speech can be delayed or absent; Seizures in the majority of individuals ( Epilepsy ); Failure to thrive in early[] […] of the corpus callosum.[] Recently mutations in the gene ZFHX1B (SIP1) were shown in patients with "syndromic Hirschsprung disease" with mental retardation (MR) and multiple congenital anomalies (MCA[]

  • Emanuel Syndrome

    The disorder involves a wide range of abnormalities such as kidney, genital and heart abnormalities, mental retardation, small head and failure to thrive.[] Affiliated tissues include heart , kidney and skin , and related phenotypes are low-set ears and agenesis of corpus callosum Genetics Home Reference : 25 Emanuel syndrome[] Multiple congenital anomalies and craniofacial dysmorphism are characterizing the so-called Emanuel or supernumerary der(22)t(11;22) syndrome (OMIM609029).[]

  • Smith Lemli Opitz Syndrome

    Affected individuals have dysmorphism, short stature, failure to thrive, microcephaly, multiple congenital malformations, and mental retardation.[] […] of corpus callosum, cerebellar vermis dysgenesis, cataracts, cleft palate, many different forms of congenital heart defect, pyloric stenosis and/or Hirschsprung dysganglionosis[] We describe a female infant with morphologic features of Rutledge multiple-congenital-anomaly syndrome (RMCAS) and biochemical features of Smith-Lemli-Opitz syndrome (SLOS[]

  • Sanjad-Sakati Syndrome

    We encountered a 2-year-old boy with hypocalcemia, failure to thrive and macrocytic anemia.[] Partial Agenesis of Corpus Callosum in Sanjad-Sakati Syndrome (p-ACC) To send this article to your Dropbox account, please select one or more formats and confirm that you[] congenital anomaly syndrome, mainly occurring in the Middle East and the Arabian Gulf countries, characterized by intrauterine growth restriction at birth, microcephaly,[]

  • Marshall-Smith Syndrome

    It is hoped that the etiology of the syndrome will be discovered as more cases are recognized and reported by pediatricians caring for infants with failure to thrive, advanced[] We describe a 5 year old patient with this rare syndrome, who has optic atrophy and agenesis of the corpus callosum, but has no respiratory problems so far.[] Syndrome of accelerated skeletal maturation in infancy, peculiar facies, and multiple congenital anomalies.[]

  • Autosomal Recessive Primary Microcephaly Type 10

    Other features include hypotonia, poor growth, lactic acidosis, and failure to thrive. The disorder may be fatal in early childhood (summary by Haack et al., 2013 ).[] congenital anomalies-hypotonia-seizures syndrome 1, 614080 PIGA Multiple congenital anomalies-hypotonia-seizures syndrome 2, 300868 MEN1 Multiple endocrine neoplasia 1, 131100[] Of The Corpus Callosum With Peripheral Neuropathy ... ...[]

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