Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome.
نویسندگان
چکیده
An inherited middle ear anomaly that was causing hearing impairment in a 12-year-old girl was treated successfully by a stapedotomy combined with a malleovestibulopexy. Cup-shaped ears, abnormal or absent thumbs, and skeletal deformities of the forearms were present in several members of 3 generations of a family. An autosomal dominant pattern of inheritance was recognized. These features are present in a number of previously described syndromes, but they correspond best with the lacrimoauriculodentodigital syndrome.
منابع مشابه
Evaluation of relationship between skin involvement and hearing loss in patients with vitiligo
Vitiligo is a common acquired depigmented disorder of the skin that can lead to social negative outcomes, including reduced quality of life. Melanocytes disorder can also occur within other organs, such as ear. Different areas of the inner ear, such as the cochlear duct and vestibular system, have melanocytes. This study was conducted with the aim of evaluating the relationship between skin inv...
متن کاملHearing Loss in Referrals of Alzahra and Edgehie Audiometry Centers in Isfahan from 1995 to 1996
Hearing loss is a major social problem and its rehabilitation is very important. Considering its prevalence in Iran, this study was performed to evaluate cases of hearing loss in referrals of Alzahra and Edgehie audiometry centers during the years 1995-1996. The descriptive strategy of this study was carried out on referrals of two audiometry clinics in Isfahan from October 1995 to 1996. Ou...
متن کاملCongenital stapes malformation: Rare conductive hearing loss in a patient with Waardenburg syndrome.
Waardenburg syndrome is a known autosomal dominant cause of congenital hearing loss. It is characterized by a distinctive phenotypic appearance and often involves sensorineural hearing loss. Temporal bone abnormalities and inner ear dysmorphisms have been described in association with the disease. However, middle ear abnormalities as causes of conductive hearing loss are not typically seen in W...
متن کاملPHACES syndrome with cataract and Horner’s syndrome: a case report
PHACES syndrome (Posterior Fossa Malformations, Hemangioma, Arterial Anomalies, Cardiac Defects and Coarctation of the Aorta, Eye Abnormalities, and Sternal Abnormalities or Ventral Developmental Defects) is a rare neurocutaneous syndrome, which characteristic feature is large segmental hemangioma. Extracutaneous involvement is an important cause of morbidity in this syndrome.<br /...
متن کاملCornelia De Lange Syndrome and Cochlear Implantation
Introduction: Literature regarding the different degrees of hearing loss in patients with Cornelia de Lange syndrome (CDLS) reports that half of the affected patients exhibit severe to profound sensorineural hearing loss. We present the first pre-school child with CDLS who underwent cochlear implantation for congenital profound sensorineural hearing loss. Case Report: A 3-year-old boy with CD...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Archives of otolaryngology--head & neck surgery
دوره 123 1 شماره
صفحات -
تاریخ انتشار 1997