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668 Possible Causes for Pendred's Syndrome

  • Pendred's Syndrome

    The sex distribution of the patients with Pendred's syndrome and their families was recorded.[ncbi.nlm.nih.gov] Acoustic structure in Pendred's syndrome was examined here by MRI for the first time.[ncbi.nlm.nih.gov] The majority of patients with Pendred's syndrome are euthyroid.[ncbi.nlm.nih.gov]

  • Goiter

    Sarcoidosis Amyloidosis Hydatidiform mole Cysts Acromegaly Pendred syndrome Goitre may be diagnosed via a thyroid function test in an individual suspected of having it.[en.wikipedia.org]

  • Autosomal Recessive Deafness 1B

    (EVA) and Pendred syndrome, which causes early hearing loss and affects the thyroid gland.[scinapse.io] […] abnormalities in BOR, or thyroid abnormalities in Pendred syndrome).[personalizedmedicine.partners.org] Pendred syndrome (PS) is the second most common type of autosomal recessive syndromic hearing loss (HL).[ncbi.nlm.nih.gov]

  • Autosomal Recessive Deafness 22

    (EVA) and Pendred syndrome, which causes early hearing loss and affects the thyroid gland.[scinapse.io] In case of recessive syndromic deafness Ushers syndrome and Pendred syndrome are most important.[ayubmed.edu.pk] syndrome (hearing loss and thyroid dysfunction), encoding a iodide-chloride transporter, may also account for an underestimated proportion of isolated deafness (DFNB4), which[ommbid.mhmedical.com]

  • X-Linked Mixed Deafness with Perilymphatic Gusher

    Baxevanis AD, Sheffield VC, Green ED (1997) Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). ‎[books.google.com] Pendred SyndromePendred syndrome an autosomal recessive disorder characterized by thyroid enlargement and sensorineural type hearing loss.[pediatric-ent.com] Syndromic Hearing Loss 32 Primary Hearing Loss Syndromes Alport Branchial-Oto-Renal Jervell and Lange-Nielsen Neurofibromatosis type 2 Pendred Waardenburg 33 Alport Syndrome[slideplayer.com]

  • Autosomal Dominant Deafness 11

    In case of recessive syndromic deafness Ushers syndrome and Pendred syndrome are most important.[ayubmed.edu.pk] syndrome (hearing loss and thyroid dysfunction), encoding a iodide-chloride transporter, may also account for an underestimated proportion of isolated deafness (DFNB4), which[ommbid.mhmedical.com] Pendred Syndrome—Pended syndrome causes sensorineural hearing loss in both ears along with thyroid problems (goiter).[verywell.com]

  • Congenital Deafness

    Patients with slowly progressing hearing loss should be checked for Alport Syndrome, Stickler Syndrome and Pendred Syndrome with a particular focus on a computed tomography[symptoma.com] Pendred Syndrome Pendred syndrome is one of the most common syndromic forms of deafness. In essence it is deafness associated with thyroid disease (euthyroid goiter).[dizziness-and-balance.com] , Jervell and Lange-Nielsen Syndrome, X-linked recessive Mohr-Tranebjaerg Syndrome, Norrie Disease, Pendred Syndrome, Stickler Syndrome, Treacher Collins Syndrome, Waardenburg[symptoma.com]

  • Autosomal Recessive Deafness 42

    In case of recessive syndromic deafness Ushers syndrome and Pendred syndrome are most important.[ayubmed.edu.pk] […] in USH2A, ADGRV1, DFNB31 Usher syndrome type III caused by pathogenic variant in CLRN1 Pendred syndrome caused by pathogenic variant in SLC26A4 Jervell and Lange-Nielsen[centogene.com] syndrome (hearing loss and thyroid dysfunction), encoding a iodide-chloride transporter, may also account for an underestimated proportion of isolated deafness (DFNB4), which[ommbid.mhmedical.com]

  • High Myopia-Sensorineural Deafness Syndrome

    […] abnormalities in BOR, or thyroid abnormalities in Pendred syndrome).[personalizedmedicine.partners.org] . [21] Pendred syndrome Pendred syndrome is the second most common type of AR syndromic hearing loss.[emedicine.medscape.com] Syndrome Most common type of AR syndromic hearing loss Congenital severe to profound SNHL Abnormality of bony labyrinth that can be diagnosed with CT scan Euthyroid goiter[en.wikibooks.org]

  • Deafness, Autosomal Dominant 23

    […] abnormalities in BOR, or thyroid abnormalities in Pendred syndrome).[personalizedmedicine.partners.org] syndrome (hearing loss and thyroid dysfunction), encoding a iodide-chloride transporter, may also account for an underestimated proportion of isolated deafness (DFNB4), which[ommbid.mhmedical.com] SIX5 Enlarged Vestibular Aqueduct (EVA) : FOXI1, KCNJ10, SLC26A4 (Pendred Syndrome) X-linked Dominant Charcot-Marie-Tooth Disease : GJB1(Cx32), TIMM8A, Chudley-McCullough[otogenetics.com]

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