{"id":12675,"date":"2024-10-11T17:38:12","date_gmt":"2024-10-11T15:38:12","guid":{"rendered":"https:\/\/valintermed.com\/?p=12675"},"modified":"2024-10-11T17:38:12","modified_gmt":"2024-10-11T15:38:12","slug":"sindrom-pendreda","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/pendreda-syndrome\/","title":{"rendered":"Pendred syndrome"},"content":{"rendered":"
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Pendred syndrome is a hereditary disorder that is caused by dysfunction of the thyroid gland and associated hearing loss. This syndrome, which belongs to a group of syndromic disorders, is characterized by auriculo-thyroid and\/or conductive hearing loss, as well as enlargement of the thyroid gland (goiter). Pendred syndrome has an autosomal recessive pattern of inheritance, which means that both parents must be carriers of the mutant alleles for the disease to manifest in offspring. Clinical manifestations are varied and can include both ear, nose and throat symptoms and endocrine disorders. The syndrome is often diagnosed in children and adolescents, which emphasizes the need for early detection and treatment in order to correct the hearing and general congenital condition of the patient.<\/p>\n

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