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12 Possible Causes for Agenesis of the Occipital Lobes, Anemia

  • Congenital Muscular Dystrophy

    A CELLULE FALCIFORMI ANEMIA CONGENITA DISERITROPOIETICA ANEMIA DI FANCONI ANEMIA SIDEROBLASTICA ANGELMAN SINDROME DI ANGIOEDEMA DI QUINCK ANGIOMA ANOMALIA MITRALICA CONGENITA[birdfoundation.org] Uncommonly, agenesis of septum pellucidum can be seen. Polymicrogyria typically seen in the frontal and parietal lobes.[neuroradiologycases.com] AGAMMAGLOBULINEMIA AICARDI SINDROME DI ALBRIGHT MALATTIA DI ALFA1-ANTITRIPSINA (AAT) DEFICIT DI ALKAPTONURIA ALLERGIE ALZHEIMER MORBO DI AMILOIDOSI ANCORAGGIO MIDOLLARE ANEMIA[birdfoundation.org]

  • Crossed Polysyndactyly

    Pre-axial polydactyly has been associated with Holt-Oram syndrome, short ribs–polydactyly syndromes, Carpenter syndrome, trisomy 21, VACTERL, and Fanconi anemia.[roentgenrayreader.blogspot.com] Computerized to- mography showed severe craniofacial anomalies, cranio- nasal dysostosis, hypertelorism, areas of pachygyria in the left occipital lobe, and agenesis of the[documentslide.com] Polydactyly may also be present in Patau's syndrome, asphyxiating thoracic dystrophy, hereditary spherocytic hemolytic anemia, Moebius syndrome, VACTERL association, and Klippel-Trenaunay[the-medical-dictionary.com]

  • Meconium Plug Syndrome

    […] and updated coverage, increased worldwide perspectives, and many new contributors keep you current on the late preterm infant, the fetal origins of adult disease, neonatal anemia[books.google.de] (A) and parietal (B) lobes on both sides Click here to view Figure 4 :Caudal regression syndrome (complete agenesis of sacrum): Frontal radiograph of the pelvis shows a contracted[ijri.org] […] an absent falx cerebri (open arrow) Click here to view Figure 3 :(A,B)Neonatal hypoglycemia: CT scan of the brain shows typical low attenuation in the white matter of the occipital[ijri.org]

  • Ring Chromosome 19

    ;q24), del(13)(q12q14) refractory anemia pter qter 7522537 2 Mitelman Database, Reference No. 5401 Edit 50 7522537_3_1 44, XY, r(3), -5, -6, r(7), add(10)(p1?)[chr7.org] […] of the corpus callosum and mild changes in the white matter in the occipital lobes; several generalized tonic-clonic seizures started at 1 year of age.[ssmc-tl.com] […] puberty, severe hirsutism amenorrhea, androgenic alopecia, clitoromegaly, diabetes, and insulin resistance–Short statureFDPMDDVentricular septal defect, severe scoliosis, anemia[edmcasereports.com]

  • Commissural Facial Cleft

    […] noma neonatorum Symptoms & signs : patients with acute noma usually present with malodorous breath, fluctuating fever (temperatures of 101 to 105 F [38 to 41 C]), marked anemia[ufrgs.br] The cephalocele sac variably includes the brainstem, occipital lobes, subarachnoid or ventricular CSF spaces, and the dural venous sinuses.[kundoc.com] The neonatal intensive care unit (NICU) course included respiratory distress syndrome, patent ductus arteriosus, sepsis, pneumonia, tracheitis, anemia, thrombocytopenia, inguinal[nature.com]

  • Autosomal Recessive Distal Osteolysis Syndrome

    Leukocytosis, anemia common with flares.[autoinflammatory-search.org] […] hypoplasia and complex malformations of the brain (cerebral and cerebellar hypoplasia, vermis, corpus callosum and/or occipital lobe agenesis, with or without arhinencephaly[mendelian.co] , Dyserythropoietic, Congenital, see congenital dyserythropoietic anemia Anemia, hereditary sideroblastic, see X-linked sideroblastic anemia anemia, hypochromic microcytic[mygenomics.com]

  • Verloove-Van Horick-Brubakk Syndrome

    Blood tests show a hypochromic microcytic anemia that is consistent with an iron-deficiency anemia.[checkrare.com] […] hypoplasia and complex malformations of the brain (cerebral and cerebellar hypoplasia, vermis, corpus callosum and/or occipital lobe agenesis, with or without arhinencephaly[mendelian.co] […] by variable signs and symptoms, mostly in infancy, including transient failure to thrive, slightly prolonged neonatal jaundice, equivocal or mild hepatomegaly, microcytic anemia[mendelian.co]

  • Lethal Arthrogryposis - Anterior Horn Cell Disease Syndrome

    , Complementation Group A Fanconi Anemia, Complementation Group C Fanconi Anemia, Complementation Group D1 Fanconi Anemia, Complementation Group E Fanconi Anemia, Complementation[sequencing.com] […] hypoplasia and complex malformations of the brain (cerebral and cerebellar hypoplasia, vermis, corpus callosum and/or occipital lobe agenesis, with or without arhinencephaly[mendelian.co] (AA) Atransferrinemia Scott syndrome Thiamine-responsive megaloblastic anemia (TRMA) Hypochromic microcytic anemia Plasminogen deficiency Rh-null hemolytic anemia (RHN) Bleeding[csirnotes.com]

  • Holoprosencephaly Type 2

    […] type 15 with mandibulofacial dysostosis RPS28 Diamond-Blackfan anemia type 14 with mandibulofacial dysostosis TSR2 DiGeorge syndrome TBX1 Donnai-Barrow syndrome LRP2 DOOR[centogene.com] […] and occipital lobes.[pediatricneurosciences.com] Semi lobar: Partial separation of the posterior occipital and temporal lobes. Frontal brain is fused, thalami partially fused.[spinwarp.ucsd.edu]

  • Pachygyria-Mental Retardation-Seizures

    […] and updated coverage, increased worldwide perspectives, and many new contributors keep you current on the late preterm infant, the fetal origins of adult disease, neonatal anemia[books.google.de] Semi lobar: Partial separation of the posterior occipital and temporal lobes. Frontal brain is fused, thalami partially fused.[spinwarp.ucsd.edu] […] to environmental stimuli, seizures, spasticity, hyperactive reflexes, tremors, “psychiatric illness” Treatment diet (no phenylalanine) leads to short stature and weight, anemia[brainaacn.org]

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