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34 Possible Causes for Hearing Impairment, Leg Length Inequality, Midline Defects

  • Malignant Hyperthermia - Arthrogryposis - Torticollis

    Midline cleft of lower lip[?] Midline defects autosomal type[?] Midline defects recessive type[?] Midline developmental field defects[?] Midline field defects[?][encyclopedia.kids.net.au] Birch, MD Leg Length Inequality Principles of Angular Deformity Correction in Children SECTION III: NEUROMUSCULAR DISORDERS 25 - Disorders of the Brain Lori A.[catdir.loc.gov] impairment Conductive deafness Conductive hearing loss [ more ] 0000405 Cryptorchidism Undescended testes Undescended testis [ more ] 0000028 Downslanted palpebral fissures[rarediseases.info.nih.gov]

  • Bladder Exstrophy

    This report provides further evidence of phenotype-genotype correlation and expands the phenotypic spectrum of midline defects described with this syndrome.[ncbi.nlm.nih.gov] Innominate osteotomy must be performed with brilliancy amplifier to avoid osteotomy through to the hip joint to prevent inequality in leg length.[ncbi.nlm.nih.gov] This is the first report of 22q11.2 microduplication associated with bladder exstrophy and hearing impairment.[ncbi.nlm.nih.gov]

  • Congenital Malformation of the Knee Joint

    […] syndrome Microphthalmia, Lenz type Microphthalmia-ankyloblepharon-intellectual disability syndrome Microphthalmia-brain atrophy syndrome Midline interhemispheric variant[se-atlas.de] In case of leg length inequality, the longer leg flexes to rebalance the pelvis.[medicus.ca] Hearing screening (Sensorineural hearing loss is associated with CP secondary to TORCH infections, meningitis.)[now.aapmr.org]

  • Acrorenal Mandibular Syndrome

    […] facial hemangioma, nerve palsies, and cardiac defects Septate uterus and vagina Teratogen Urogenital adysplasia Unilateral or bilateral renal agenesis, flattened facies,[omicsonline.org] Length Inequality Lenz Majewski Hyperostotic Dwarfism Lissencephaly Type III and Bone Dysplasia Macroepiphyseal Dysplasia, McAlister Coe Type Marfan syndrome Marfan Syndrome[rgd.mcw.edu] hearing impairment and Renal hypoplasia Symptoms // Phenotype % cases Hearing impairment Very Common - Between 80% and 100% cases Pica Common - Between 50% and 80% cases[mendelian.co]

  • Deafness-Epiphyseal Dysplasia-Short Stature Syndrome

    Failure of ossification of midline junction of bones Treatment Little if any functional defect Coxa vara if present may require osteotomy Pyknodysostosis Inheritance Autosomal[flinders.edu.au] Signs and Symptoms Hearing impairment ... ...[familydiagnosis.com] […] syndrome Microphthalmia, Lenz type Microphthalmia-ankyloblepharon-intellectual disability syndrome Microphthalmia-brain atrophy syndrome Midline interhemispheric variant[se-atlas.de]

  • Familial Congenital Nasolacrimal Duct Obstruction

    Surgical treatment consists of complete removal of the mass--both intracranial and intranasal--with closure of the resulting defect.[myslide.es] Dermatoses Leg Injuries Leg Length Inequality Leg Ulcer Legg-Perthes Disease Legionellosis Legionnaires' Disease Leigh Disease Leiomyoma Leiomyoma, Epithelioid Leiomyomatosis[medgene.med.harvard.edu] Intellectual disability Pica Hearing impairment Nystagmus SOURCES: OMIM UMLS MONDO ORPHANET GARD More info about COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT[mendelian.co]

  • Autosomal Dominant Mental Retardation Type 21

    The associated scalp defects are midline skin defects located on the vertex with occasional defects of the skull and meninges.[oandplibrary.org] Length Inequality Lenz Majewski Hyperostotic Dwarfism LEOPARD syndrome Leri-Weill dyschondrosteosis Lethal Congenital Nonspherocytic Hemolytic Anemia with Genital and Other[rgd.mcw.edu] Complete Probemix List New and Improved Products IVD-Registered Products Bacteria Blood Cancers Cardiovascular Carrier Endocrine & Reproductive Gastrointestinal & Liver Hearing[mlpa.com]

  • Congenital Absence of Thigh and Lower Leg with Foot Present

    Parieto-occipital DSTs more frequently have intracranial extension through a midline occipital skull defect, penetrate the dura, and end intracranially in relation to either[pediatrics.aappublications.org] Leg length inequality. Journal of Manipulative and Physiological Therapeutics. 15(9): 576-90. McCaw, S.T. Leg length inequality.[veterans.gc.ca] Other neurological symptoms that commonly occur in individuals with CP include seizures, hearing loss and impaired vision, bladder and bowel control issues, and pain and abnormal[childneurologyfoundation.org]

  • Cardio-Spondylo-Carpo-Facial Syndrome

    Midline defects, including hypoplastic or aplastic clavicles with hypermobile shoulders, short middle phalanges, coxa vara, symphysis pubis diastasis, scoliosis, and spondylolisthesis[musculoskeletalkey.com] Expertise, Disease and Conditions: Achondroplasia, Blount's Disease, Cerebral Palsy, Fractures, Hip Dislocations, Hip Dysplasia, Kyphosis, Leg Length Inequality, Marfan Syndrome[hopkinsmedicine.org] […] recessive lysosomal storage disease characterized by mental retardation, coarse facial features, skeletal abnormalities, hearing impairment, neurologic motor problems, and[mendelian.co]

  • Schwartz-Lelek Syndrome

    Failure of ossification of midline junction of bones Treatment Little if any functional defect Coxa vara if present may require osteotomy Pyknodysostosis Inheritance Autosomal[flinders.edu.au] […] and Conductive hearing impairment that can help you solving undiagnosed cases.[mendelian.co] impairment Respiratory distress Craniofacial hyperostosis Prominent supraorbital ridges Global developmental delay Facial hyperostosis Conductive hearing impairment Abnormal[mendelian.co]

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