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327 Possible Causes for Agenesis of Corpus Callosum, Failure to Thrive, Recurrent Bacterial Infection

  • Sanjad-Sakati Syndrome

    A similar syndrome with the additional features of osteosclerosis and recurrent bacterial infections has been classified as autosomal recessive Kenny-Caffey syndrome (AR-KCS[] 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[]

  • Kenny-Caffey Syndrome Type 1

    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.[] CASE REPORT A 7-month-old girl was admitted to the children hospital in Damascus for the first time complaining of failure to thrive.[] It is similar to hypoparathyroidism-retardation-dysmorphism syndrome, with the additional findings of osteosclerosis and recurrent bacterial infections.[]

  • Autosomal Recessive Primary Microcephaly Type 10

    infections, recurrent, due to MYD88 deficiency, 612260 PSTPIP1 Pyogenic sterile arthritis, pyoderma gangrenosum, and acne, 604416 PNPO Pyridoxamine 5-phosphate oxidase deficiency[] 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 ).[] Pyogenic bacterial infections, recurrent, due to MYD88 deficiency, 612260 (3) MYEOV G:605625 . . MYF5 G:159990 . . MYF6 G:159991 .[]

  • Wolf-Hirschhorn Syndrome

    […] of the corpus callosum, bilateral renal hypoplasia, and two atrial septal defects.[] 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[] We should consider autoinflammatory disorders in the differential diagnosis of recurrent fever even if the patients have a congenital disease susceptible to bacterial infections[]

  • Kostmann Syndrome

    Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum Nicolas Dupré, Heidi C Howard, and Guy A Rouleau.[] Patients present with an enlarged liver and spleen, failure to thrive, kidney problems, hypoglycaemia (low blood sugar) and recurrent infections.[] bacterial infections (e.g. otitis media, pneumonia, sinusitis, urinary tract infections, abscesses of skin and/or liver) and increased promyelocytes in the bone marrow.[]

  • Encephalocele

    Agenesis or hypogenesis of the corpus callosum is a commonly associated finding.[] […] to thrive are seen.[] Abstract Bacterial meningitis is a life-threatening infection with a low recurrence rate. However, this possibility has always to be considered and avoided.[]

  • Erythroderma Desquamativum

    […] diarrhoea, recurrent skin and internal infections, and failure to thrive.[] Blogs Submit your blog on Generalized Erythroderma, Diarrhea, And Failure To Thrive to be featured![] […] of Corpus Callosum Agranulocytosis, Acquired Ahumada-Del Castillo Syndrome Aicardi Syndrome AIDS (Acquired Immune Deficiency Syndrome) AIDS Dysmorphic Syndrome Alagille Syndrome[]

  • Lymphopenic Agammaglobulinemia - Short-Limbed Dwarfism Syndrome

    infectionRecurrent stomatitis, Gingivitis and Otitis 37.[] […] to thrive).[] […] of Cerebral White Matter OMIM:613623 Agenesis of the Corpus Callosum and Congenital Lymphedema OMIM:218000 Agenesis of the Corpus Callosum with Peripheral Neuropathy; ACCPN[]

  • Glycogen Storage Disease due to Glucose-6-Phosphat Transport Defect

    In addition, they are susceptible to recurrent bacterial infection and have recurrent oral ulcers and occasionally Crohn’s-like disease.[] Of Corpus Callosum With Neuronopathy Agenesis Of Corpus Callosum With Peripheral Neuropathy Agenesis Of Corpus Callosum With Polyneuropathy Charlevoix Disease Hereditary[] […] to thrive In neuromuscular forms, hypotonia and muscle atrophy Treatment: None known For cirrhosis, liver transplantation, which treats the primary disease as well GSD V[]

  • Holoprosencephaly - Recurrent Infections - Monocytosis

    Recurrent bacterial and fungal infections (less severe than LAD-I).[] Affected individuals had microcephaly, severe developmental delay, failure to thrive, and brachydactyly.[] […] of the corpus callosum mental retardation, severe interhemispheric cysts Genitourinary External Genitalia Male: micropenis Head And Neck Eyes: epicanthal folds Laboratory[]

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