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994 Possible Causes for Agenesis of Corpus Callosum, Failure to Thrive, Small Hand

  • Sanjad-Sakati Syndrome

    We encountered a 2-year-old boy with hypocalcemia, failure to thrive and macrocytic anemia.[] All patients had severe intrauterine growth retardation, short stature, small hands and feet, blue sclera, deep-set eyes, microcephaly, persistent hypocalcaemia and hypoparathyroidism[] 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[]

  • Prader-Willi Syndrome

    Prader-Willi syndrome (PWS) is characterized by infantile lethargy and hypotonia causing poor feeding and failure to thrive, childhood obesity, short stature, and hypogonadism[] hands and feet, mild dysmorphology, and behavior problems which can be severe.[] In addition Hirschsprung disease, congenital cardiac defects and agenesis of the corpus callosum may be associated with mutations in ZFHX1B.[]

  • Lissencephaly

    Symptoms of the disorder may include unusual facial appearance, difficulty swallowing, failure to thrive, muscle spasms, seizures, and severe psychomotor retardation.[] Babies born with lissencephaly may have an abnormally small head, a condition known as microlissencephaly. But not all babies with lissencephaly have this appearance.[] MRI showed diffuse pachygyria, moderate thickening of the cortex, enlarged ventricles, agenesis of the corpus callosum and septum pellucidum.[]

  • 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[] “When Lindsay smiles with delight and her face glows with happiness or when she places her small hand in mine as we walk together, I am truly filled with joy … We certainly[] 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.[]

  • Lenz-Majewski Syndrome

    The disorder is characterized by failure to thrive and mental retardation.[] Absent/small middle finger bone of the hand Absent/underdeveloped middle finger bone of the hand [ more ] 0009843 Autosomal dominant inheritance 0000006 Broad clavicles Broad[] […] to thrive, mental retardation, sparse hair, enamel hypoplasia, loose skin, and skeletal abnormalities.[]

  • Kenny-Caffey Syndrome Type 1

    CASE REPORT A 7-month-old girl was admitted to the children hospital in Damascus for the first time complaining of failure to thrive.[] hands and feet, hypocalcaemia, hypoparathyroidism, radiologic evidence of cortical thickening of long bones with medullary stenosis, and absent diploic space in the skull[] Khan Partial agenesis of corpus callosum in Sanjad–Sakati syndrome (p-ACC) Can J Neurol Sci, 39 (2012), pp. 833-834 [3] S. Sanjad, N.A. Sakati, Y. Abu-Osba, R.[]

  • 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[] […] distal phalanges in the hands, so-called brachytelephalangy and nasomaxillary hypoplasia.[] […] of corpus callosum microcephaly microphthalmia congenital cataracts cardiovascular congenital cardiac anomalies Warfarin is a teratogenic drug.[]

  • Growth Failure

    Presentation on theme: "Faltering growth(failure to thrive)"— Presentation transcript: 1 Faltering growth(failure to thrive) refers to not only failure of growth(suboptimal[] The strip is put into a glucometer-a small hand-held device to measure the blood sugar level.[] Cranial defects may present with wide heads, flat noses, cleft lip/palate, hypertelorism, agenesis of the corpus callosum, hypopituitarism, posterior pituitary ectopia, basal[]

  • Goldberg-Shprintzen Syndrome

    Hirschsprung disease can eventually cause diarrhea, dehydration, and failure to grow and gain weight at the expected rate (failure to thrive).[] Additional dysmorphic features may include maxillary hypoplasia, hypodontia, high arched palate, short neck, small hands, brachydactyly, fifth finger clinodactyly, fetal finger[] Since agenesis of the corpus callosum is the only MWS feature that can be detected prenatally, molecular screening of the ZEB2 gene in prenatal isolated agenesis of the corpus[]

  • CAMFAK Syndrome

    Diseases related to Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome via text searches within MalaCards or GeneCards Suite gene sharing: Human phenotypes[] & unsteady gait. other symptoms include seizures, optic atrophy, farsightedness, slender nose, thin skin, cool feet & hands, thin hair, small pelvis, weakness, incoordination[] There was associated partial agenesis of the corpus callosum.[]

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