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52 Possible Causes for Congenital Ear Deformity, Ectopia Lentis, Facial Nerve Disorder

  • CHARGE Syndrome

    (congenital) 759.89 Ullrich-Feichtiger syndrome 759.89 VATER syndrome 759.89 Weill-Marchesani syndrome (brachymorphism and ectopia lentis) 759.89 "Whistling face" syndrome[icd9data.com] lentis) 759.89 Menkes' 759.89 Meyer-Schwickerath and Weyers (dysplasia oculodentodigitalis) 759.89 microphthalmos (congenital) 759.89 Mieten's 759.89 Mohr's (types I and[icd9data.com] lentis 759.89 Bruck-de Lange disease or syndrome (Amsterdam dwarf, intellectual disabilities, and brachycephaly) 759.89 Carpenter's syndrome 759.89 Cerebrohepatorenal syndrome[icd9data.com]

  • Thickened Earlobes-Conductive Deafness Syndrome

    Disorders of the facial nerve. Gleeson M, Browning GG, Burton MJ et al. Scott Brown’s Otolaryngology, Head and neck surgery. 7.[emedicine.medscape.com] lentis isolated Ectopia pupillae Ectopic coarctation Ectopic ossification familial type Ectopic pregnancy Ectrodactyly cardiopathy dysmorphism Ectrodactyly cleft palate syndrome[bioreference.net] Deformities Absence of the outer ear Congenital deformity or absence of the outer ear, usually on one side, sometimes on both, is often accompanied by absence of the outer-ear[britannica.com]

  • Acrootoocular Syndrome

    […] of facial nerve Congenital facial asymmetry Congenital facial nerve palsy Congenital hydronephrosis Congenital hypertrichosis Congenital hypogonadotropic hypogonadism Congenital[icdlist.com] Congenital lens dislocation/AD/FBN1/#129600 ECTOPIA LENTIS, ISOLATED/Lens dislocation/AR/ADAMTSL4/#225100 EHLERS-DANLOS SYNDROME /Myopia, ectopia lentis, blue sclera, epicanthal[eyewiki.org] Microtia - Congenital Ear Institute evaluates and operates hundreds of children born with a congenital ear deformity known as microtia/atresia ...[ibis-birthdefects.org]

  • Familial Recurrent Peripheral Facial Palsy

    Facial palsy: unusual etiology . Laryngoscope 1977 ; 87 : 26 – 34 61 May , M , Hughes , GB . Facial nerve disorders: update 1987 .[cambridge.org] lentis-microspherophakia-stiff joints-short stature syndrome Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Glaucoma-sleep apnea syndrome GLB1 deficiency[orpha.net] : Anteverted nostrils, Malformed and low-set ears Developmental delay: Mild Poland syndrome: 1 patient Congenital heart disease Atrial septal defects Similar genetic changes[neuromuscular.wustl.edu]

  • Congenital Entropion

    Lagophthalmos Causes of lagophthalmos Common cause – facial nerve paralysis Other causes – related to cicatricial changes of the eyelids due to chemical/thermal injury or[kjophthal.com] Lentis 232 Traumatic Luxation 234 Basic Mechanisms of Cataract Formation 236 Basic Aspects of Cataract Surgery 244 Extracapsular Cataract Extraction 245 Intracapsular Cataract[books.google.com] ICD-CODE.org Codes Chapters Blocks Categories Congenital malformations, deformations and chromosomal abnormalities Congenital malformations of eye, ear, face and neck Q10[icd-code.org]

  • Malformations of the Auditory Ossicles

    First arch contributes to incus, malleus, tensor tympani muscle, and mandible, and second arch to stapes, facial nerve canal, stapedius muscle, and the styloid process.[ijri.org] Marfan's - AD, mixed HL, scoliosis, arachnodactyly, ectopia lentis, cardiovascular abnormalities.[en.wikibooks.org] ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q10-Q18 Congenital malformations of eye, ear, face and neck › Q16- Congenital[icd10data.com]

  • Familial Congenital Nasolacrimal Duct Obstruction

    […] affecting eyelid function Excludes: blepharoclonus (333.81) blepharospasm (333.81) facial nerve palsy (351.0) third nerve palsy or paralysis (378.51-378.52) tic (psychogenic[theodora.com] (congenital) 759.89 Ullrich-Feichtiger syndrome 759.89 VATER syndrome 759.89 Weill-Marchesani syndrome (brachymorphism and ectopia lentis) 759.89 "Whistling face" syndrome[icd9data.com] Small, deformed, or low-set auricles may indicate associated congenital defects,especially renal disease.[quizlet.com]

  • Familial Congenital Palsy of Trochlear Nerve

    Home, Search, Index, Links, Pathology, Molecules, Syndromes, Muscle, NMJ, Nerve, Spinal, Ataxia, Antibody & Biopsy, Patient Info FACIAL (VII) NERVE DISORDERS Facial nerve:[neuromuscular.wustl.edu] lentis-chorioretinal dystrophy-myopia syndrome Endophthalmitis Endotheliitis Essential iris atrophy Familial benign flecked retina Familial congenital palsy of trochlear[se-atlas.de] (CCDDs) which are neurological disorders affecting one or more of the 12 cranial nerves.[clinicaltrials.gov]

  • Rieger Syndrome

    It is characterized by an ipsilateral third nerve paralysis associated with facial paralysis and contralateral hemiplegia.[medical-dictionary.thefreedictionary.com] By Genes Gene (MIM#) Chromosome Location Disease CYP1B1 (601771) 2p21 Primary congenital glaucoma FBN1 / fibrillin (134797) 15q21 Ectopia Lentis (simple) FKHL7 (601090) 6p25[glaucoma.net] ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q10-Q18 Congenital malformations of eye, ear, face and neck › Q13- Congenital[icd10data.com]

  • Infantile Choroidocerebral Calcification Syndrome

    Synonyms: fourth phacomatosis ('mother-spot') or encephalotrigeminal angiomatosis Sturge-Weber syndrome (SWS) is a neurocutaneous disorder classically presenting with: A facial[patient.info] lentis - chorioretinal dystrophy - myopia Ectopia lentis isolated 6,4 Ectrodactyly - ectodermal dysplasia EEM syndrome Ehlers-Danlos syndrome type 10 7 families Ehlers-Danlos[docplayer.net] May be associated with Chiari malformation, syrinx, renal, spinal cord, inner/middle/outer-ear abnormalities, congenital heart disease. 1/3 also have Sprengel’s deformity[radnotes.co.nz]

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