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48 Possible Causes for Bilateral Congenital Profound Sensorineural Hearing Loss, Delayed Speech Development

  • Congenital Deafness

    hearing loss ranges from mild to profound hearing loss.[wvdhhr.org] This results in delayed speech/language development, social problems and academic difficulties.[pamf.org] Parental concerns about possible hearing loss or observed delays in speech development require auditory screening in any child.[ncbi.nlm.nih.gov]

  • Microtia

    […] canals, and bilateral profound sensorineural hearing loss (HL).[ncbi.nlm.nih.gov] Studies report delayed speech development and academic difficulties in children with a conductive hearing loss, and stress the importance of early intervention not only in[newcastle-hospitals.org.uk] Even if no hearing device is used, the child should still develop normal speech and language because of the normal hearing in the unaffected ear.[everydayhearing.com]

  • Long QT Syndrome

    The Jervell and Lange-Nielsen syndrome is an autosomal recessive form of LQTS and is characterized by congenital profound bilateral sensorineural hearing loss and long QT[medicinenet.com] Delays in treatment for profound sensorineural hearing loss will result in the inability for the patient to develop normal spoken speech and language skills.[californiaearinstitute.com] In some cases, LQTS may be associated with congenital profound bilateral sensorineural hearing loss, known as Jervell and Lange-Nielsen syndrome (JLNS).[mayomedicallaboratories.com]

  • Deafness

    Mumps (Epidemic parotitis) may result in profound sensorineural hearing loss (90 dB or more), unilateral (one ear) or bilateral (both ears). congenital rubella (also called[en.wikipedia.org] Parental concerns about possible hearing loss or observed delays in speech development require auditory screening in any child.[ncbi.nlm.nih.gov] […] is delayed in developing speech or has unclear speech; turns the volume up loud on the TV and other electronic devices. ( American Speech-Language-Hearing Association , n.d[readingrockets.org]

  • Usher Syndrome Type 1

    , profound sensorineural hearing loss, adolescent-onset retinitis pigmentosa and loss of vestibular function.[ltd.aruplab.com] A common early symptom may be the delayed development of speech.[retinaaustralia.com.au] Diagnostic methods Clinical diagnosis is based on findings of bilateral sensorineural hearing loss (symmetric, congenital and profound for type 1, and moderate to severe with[orpha.net]

  • Autosomal Recessive Deafness 24

    […] born with profound congenital deafness.[vdocuments.site] Differential Diagnosis In children with delayed speech development, the auditory system should be assessed.[bredagenetics.com] Parental concerns about possible hearing loss or observed delays in speech development require auditory screening in any child.[ncbi.nlm.nih.gov]

  • Autosomal Recessive Deafness 38

    […] born with profound congenital deafness.[vdocuments.site] MRT38 is characterized by global developmental delay affecting motor, speech, adaptive, and social development.[uniprot.org] Parental concerns about possible hearing loss or observed delays in speech development require auditory screening in any child.[ncbi.nlm.nih.gov]

  • Long QT Syndrome 8

    Jervell and Lange-Nielsen syndrome (JLNS) is characterized by congenital profound bilateral sensorineural hearing loss and LQTc usually greater than 500 msec.[ncbi.nlm.nih.gov] Affected children tend to have impaired communication and socialization skills, as well as delayed development of speech and language.[ghr.nlm.nih.gov]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    , bilateral, profound sensorineural hearing loss, vestibular areflexia, and adolescent-onset retinitis pigmentosa.[refsumdisease.org] Delayed motor skill development, poor balance and slurred speech are typically the first indications of the disease.[mayoclinic.org] (See also the GeneReview: Retinitis Pigmentosa Overview.) 2b(iii) Retinitis pigmentosa and sensorineural hearing loss Usher syndrome type 1 is characterized by a congenital[refsumdisease.org]

  • Autosomal Dominant Deafness 33

    […] born with profound congenital deafness.[docslide.net] Differential Diagnosis In children with delayed speech development, the auditory system should be assessed.[bredagenetics.com] Parental concerns about possible hearing loss or observed delays in speech development require auditory screening in any child.[consilieregenetica.org]

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