Create issue ticket

209 Possible Causes for Microtia Type 1

  • Microtia

    There are 4 types of microtia. ranging from Type 1 to Type 4.[health.state.mn.us] There are four different types of microtia, ranging from type 1, the mildest form, to type 4, the most severe. What causes microtia?[childrenshospital.org] Type 1 microtia is the mildest, usually with a smaller-than-normal ear that has most of the components of a non-affected ear.[health.state.mn.us]

  • Anotia

    There are 4 types of microtia. ranging from Type 1 to Type 4.[health.state.mn.us] Four types of Microtia exist, ranging in severity from Type 1 to Type 4.[sexner.com] Type 1 microtia is the mildest, usually with a smaller-than-normal ear that has most of the components of a non-affected ear.[health.state.mn.us]

  • Familial Recurrent Peripheral Facial Palsy

    1 Hyperprolinemia type 2 Hypertelorism-microtia-facial clefting syndrome Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome[se-atlas.de] […] encephalopathy due to adenosine kinase deficiency Hyperphenylalaninemia due to tetrahydrobiopterin deficiency Hyperphosphatasia-intellectual disability syndrome Hyperprolinemia type[se-atlas.de]

  • Deafness with Labyrinthine Aplasia - Microtia - Microdontia

    1 Thanatophoric dysplasia type 2 Synonym(s): - LAMM syndrome - Microdontia - type I microtia - deafness Classification (Orphanet): - Rare developmental defect during embryogenesis[csbg.cnb.csic.es] She presented with type 1 microtia, widely spaced small teeth ( Fig .1 ), and genu valgum. Neurological examination was normal.[indianpediatrics.net] The proband was a 4-year-old girl, who presented with prominent tip of the nose, dysplastic ears, bilateral type 1 microtia, and microdontia with widely spaced teeth.[cags.org.ae]

  • Congenital Mandibular Hypoplasia

    Among them, the OAV spectrum followed by the mandibulofacial dysostosis (MFD) group or TCS comprises the most common types and hence requires a short discussion. [1] The oculo-auriculo-vertebral[jofs.in] […] spectrum The OAV includes a broad spectrum of anomalies ranging from isolated microtia to Goldenher syndrome.[jofs.in]

  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    1 Hyperprolinemia type 2 Hypertelorism-microtia-facial clefting syndrome Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome[se-atlas.de] […] encephalopathy due to adenosine kinase deficiency Hyperphenylalaninemia due to tetrahydrobiopterin deficiency Hyperphosphatasia-intellectual disability syndrome Hyperprolinemia type[se-atlas.de]

  • Distal Hereditary Motor Neuropathy Type 1

    1 Hyperprolinemia type 2 Hypertelorism-microtia-facial clefting syndrome Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome[se-atlas.de] […] encephalopathy due to adenosine kinase deficiency Hyperphenylalaninemia due to tetrahydrobiopterin deficiency Hyperphosphatasia-intellectual disability syndrome Hyperprolinemia type[se-atlas.de]

  • Hereditary Hyperekplexia

    , hearing impairment, and cleft palate) HOXD10 (Vertical talus, congenital) HOXD13 (Brachydactyly type D) HPD (Hawkinsinuria) HPGD (Cranioosteoarthropathy) HPRP3 (Retinitis[en.praenatal-medizin.de] (MODY, type I) HOXA1 (Athabaskan brainstem dysgenesis syndrome) HOXA11 (Radioulnar synostosis with amegakaryocytic thrombocytopenia) HOXA13 (Guttmacher syndrome) HOXA2 (Microtia[en.praenatal-medizin.de] […] pigmentosa-18) HPRT1 (HPRT-related gout) HPS1 (Hermansky-Pudlak syndrome 1) HPS3 (Hermansky-Pudlak syndrome 3) HPS4 (Hermansky-Pudlak syndrome 4) HPS5 (Hermansky-Pudlak syndrome[en.praenatal-medizin.de]

  • X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome

    1 Hyperprolinemia type 2 Hypertelorism-microtia-facial clefting syndrome Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome[se-atlas.de] […] encephalopathy due to adenosine kinase deficiency Hyperphenylalaninemia due to tetrahydrobiopterin deficiency Hyperphosphatasia-intellectual disability syndrome Hyperprolinemia type[se-atlas.de]

  • Autosomal Recessive Deafness 24

    , sensorineural, mitochondrial MT-RNR1 Deafness, X-linked type 1 PRPS1 Deafness, X-linked type 2 POU3F4 Deafness, X-linked type 4 SMPX Deafness, X-linked type 5 AIFM1 Deafness[centogene.com] 12 CDH23 Deafness, congenital with inner ear agenesis, microtia, and microdontia FGF3 Deafness, dystonia, and cerebral hypomyelination, X-linked BCAP31 Deafness, nonsyndromic[centogene.com] TBC1D24 Deafness, autosomal recessive type 89 KARS Deafness, autosomal recessive type 91 SERPINB6 Deafness, autosomal recessive type 93 CABP2 Deafness, autosomal recessive, type[centogene.com]

Further symptoms