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16 Possible Causes for Congenital Deafness, Icterus Gravis Neonatorum

  • Fetal Erythroblastosis

    […] disease hemolytic newborns , erythroblastosis fetalis , disease hemolytic newborn , disease hemolytic of newborn , diseases hemolytic newborn , icterus gravis neonatorum ,[fpnotebook.com] Plasmapheresis was given from 17 weeks of gestation but fetal erythroblastosis still developed 1 week later.[ncbi.nlm.nih.gov] OBJECTIVE: This study was designed to test our hypothesis that fetal erythroblastosis may be a risk factor for developing THI.[ncbi.nlm.nih.gov]

  • Fetal Hypoxia

    erythroblastosis) are a serious and complex medical condition of the fetus and the newborn,… Neonatology If your premature baby but before SSW 32 to the world, it is always[de.pons.com] […] der Neonatologie, der Klinik für Frühgeborene, betreut. de.mimi.hu Under the Hemolytic disease of the newborn ( also : Fetopathia serologica, erythroblastosis fetalis or fetal[de.pons.com]

  • Dilated Cardiomyopathy Type 2B

    […] type DFNB Bethlem myopathy Chilblain lupus Congenital muscular dystrophy, Ullrich type Corpus callosum agenesis - neuronopathy Early-onset myopathy with fatal cardiomyopathy[csbg.cnb.csic.es] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] […] pads, deafness AND leukonychia syndrome Leber congenital amaurosis 1 Leber congenital amaurosis 10 Leber congenital amaurosis 11 Leber congenital amaurosis 13 Leber congenital[pentacorelab.hu]

  • Bencze Syndrome

    Congenital corneal dystrophy, progressive sensorineural deafness in a family. Arch Ophthalmol 1971; 85:27-32. Kirkness CM, et al.[dentisty.org] Bowen's disease Bowing congenital short bones[?] Bowing of long bones congenital[?] Boylan Dew Greco syndrome[?] Brachioskeletogenital syndrome[?][encyclopedia.kids.net.au] Brachyc * Brachycephalofrontonasal dysplasia * Brachycephaly deafness cataract mental retardation Brachyd * Brachydactylous dwarfism Mseleni type Brachydactyly * Brachydactyly[en.academic.ru]

  • Nelson Syndrome

    deafness.[ahajournals.org] Gravis Neonatorum[mesh.kib.ki.se] Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death. Am Heart J. 1957 ; 54 :59–68. Crossref Medline Google Scholar 5.[ahajournals.org]

  • Blue Diaper Syndrome

    Syndrome, Type 4A, Neonatal, with Sensorineural Deafness) 601678 (Bartter Syndrome, Type 1, Antenatal) 613743 (Adrenal insufficiency, congenital, with 46,XY sex reversal,[hmdb.ca] Kidney Int. 2006 Jun;69(11):2064-9. [ PubMed:16572107 ] Badalian SS, Mikhailov AV: [Characteristics of the renin-aldosterone system of the fetoplacental complex in fetal erythroblastosis[hmdb.ca] […] partial or complete) 241200 (Bartter Syndrome, Type 2, Antenatal) 613090 (Bartter Syndrome, Type 4B, Neonatal, With Sensorineural Deafness) 604278 (Renal tubular acidosis[hmdb.ca]

  • Autosomal Dominant Classic Optic Atrophy

    Dominant ER Stress-Inducing WFS1 Mutations Underlie a Genetic Syndrome of Neonatal/Infancy Onset Diabetes, Congenital Sensorineural Deafness and Congenital Cataracts , Sarah[diabetes.diabetesjournals.org] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] Two variants of LQTS have been described: a rare recessive form with congenital deafness (Jervell and Lange-Nielsen syndrome, J-LN), and a more frequent autosomal dominant[aetna.com]

  • Classic Autosomal Dominant Optic Atrophy

    […] or early-onset sensorineural deafness, and congenital cataracts.[diabetes.diabetesjournals.org] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Blood Genotyping RH C, Hemolytic Disease[aruplab.com] The availability of molecular testing has revealed phenotypic variations, such as severe congenital forms of optic atrophy [ 16 ], ADOA associated with sensorineural deafness[molvis.org]

  • Northern Epilepsy

    […] hemiplegic migraine type 2 Spondyloepimetaphyseal dysplasia with hypotrichosis Maxillonasal dysplasia, Binder type Osteopetrosis Albinism ocular late onset sensorineural deafness[checkrare.com] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] […] disorder of glycosylation, Type IB Congenital myasthenic syndrome, CHRNE-associated Congenital myasthenic syndrome, RAPSN-associated CRB1-associated retinal dystrophies Crigler-Najjar[genpathdiagnostics.com]

  • X-Linked Syndromic Mental Retardation Type 12

    (disorder) {719102004 , SNOMED-CT } Congenital cataract with deafness and hypogonadism syndrome (disorder) {722378009 , SNOMED-CT } Congenital cataract with hypertrichosis[phinvads.cdc.gov] erythroblastosis, isoimmunization, alloimmune hemolytic 0050421 RhCc Antigen ( RHCE ) Genotyping Additional Technical Information Rh Genotyping RH C, Hemolytic Disease of[aruplab.com] Two variants of LQTS have been described: a rare recessive form with congenital deafness (Jervell and Lange-Nielsen syndrome, J-LN), and a more frequent autosomal dominant[aetna.com]

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