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189 Possible Causes for Clenched Hands, Congenital Heart Disease, Syndactyly

  • Pierre Robin Syndrome

    Abstract In reviewing eight cases of children with the Pierre Robin syndrome, we found three cases to have abnormalities of the extremities such as syndactyly, hypoplastic[ncbi.nlm.nih.gov] Symptoms include cleft lip or palate, clenched hands (with outer fingers on top of the inner fingers), close-set eyes, decreased muscle tone, extra fingers or toes (polydactyl[doi.org] Congenital heart disease occurs in about 20 percent of patients with Pierre Robin syndrome.[ncbi.nlm.nih.gov]

  • Cornelia De Lange Syndrome

    Congenital heart disease (CHD) is not a major criterion of the disease, but it affects many individuals.[ncbi.nlm.nih.gov] Interestingly, the upper limbs are typically much more involved than the lower extremities that generally manifest with small feet and 2-3 syndactyly of the toes and shortened[ncbi.nlm.nih.gov] […] contrast, other features characteristic of isochromosome 18p, namely microstomia, prominent upper lip, pinched nose, asymmetric long face, long and narrow fingers/toes, clenched[jmg.bmj.com]

  • Trisomy 18

    A prenatal diagnosis of ductal-dependent, complex congenital heart disease was made in a fetus with trisomy 18.[ncbi.nlm.nih.gov] The case of a newborn male with trisomy 18 syndrome, having bilateral syndactyly, aplasia and hypoplasia of the foot digits, unilateral ectrodactyly of the left foot and a[ncbi.nlm.nih.gov] At least 30% of affected fetuses have abnormal extremities (unilateral or bilateral), the most frequent one being clenched hand and radial aplasia.[humpath.com]

  • Apert Syndrome

    Surgical correction of syndactyly of the Apert hand should begin by 6 months and be completed by 3 years of age.[ncbi.nlm.nih.gov] Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18.[eyewiki.aao.org] Apert syndrome (AS) is a rare autosomal dominant disorder characterised by craniosynostosis and limb malformations, and is associated with congenital heart disease and other[ncbi.nlm.nih.gov]

  • Patau Syndrome

    Most infants with trisomy 13 have congenital heart disease.[nlm.nih.gov] She had rocker-bottom feet, with convex soles, and syndactyly of the third and fourth fingers in both feet, with retraction of the second finger.[funpecrp.com.br] hand with finger overlap, rocker bottom feet, micrognathia, low set ears Image depicting classic appearance of clenched hand with overlapping 2nd and 5th fingers in a newborn[pedclerk.bsd.uchicago.edu]

  • Ellis-Van Creveld Syndrome

    Other features noted in the girls were syndactyly and mild mitral regurgitation.[ncbi.nlm.nih.gov] Limitation of hand function, such as the inability to form a clenched fist, is frequently observed.[emedicine.com] In 1940 Ellis and van Creveld (2) described 2 more patients with similar congenital anomalies who, in addition, had congenital heart disease.[annals.org]

  • Partial Trisomy 13 in Patau Syndrome

    […] palate; microcephaly (small head); small, sometimes fused eyes; low set ears; micrognathia (small lower jaw); a variety of cardiac defects; umbilical and/or inguinal hernias; syndactyly[actforlibraries.org] hands with overlapping fingers decreased muscle tone abnormal forebrain structures holoprosencephaly polydactyly cryptorchidism congenital heart disease "punched out" lesions[medbullets.com] […] cleft lip or cleft palate small skull (microcephaly) malformations of the hands and feet – including missing thumbs, club feet and webbing between the fingers and toes (syndactyly[betterhealth.vic.gov.au]

  • Crouzon Syndrome

    Child had episodes of cyanosis while crying for which he was evaluated by cardiologist and congenital cyanotic heart diseases were ruled out.[jnaccjournal.org] Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome.[ncbi.nlm.nih.gov] Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18.[ncbi.nlm.nih.gov]

  • Short stature-Valvular Heart Disease-Characteristic Facies Syndrome

    Diagnosis and Management of Adult Congenital Heart Disease, by Drs.[books.google.com] Telecanthus Toe syndactyly Thin vermilion border Delayed eruption of teeth Microcornea Hypoplasia of the maxilla Small hand Short palpebral fissure Camptodactyly Conductive[mendelian.co] […] consist of 45X mosaicism and X structural abnormalities.173 Patients with severe dysmorphic features have a significantly higher prevalence of congenital heart disease,173[mitchmedical.us]

  • Syndactyly

    This study reports the first frameshift mutation in the BHLHA9 causing mesoaxial synostotic syndactyly and phalangeal reduction.[ncbi.nlm.nih.gov] I do however have some difficulties anatomically with some hand movements, such as: gripping (as my right hand is slightly smaller than my left), clenching a fist (not that[goodmenproject.com] heart disease amongst others.[ncbi.nlm.nih.gov]

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