MeSH 搜索器

Branchio-Oto-Renal Syndrome

An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)
推出的年份: 1997
副标题
树号: C16.131.077.208, C16.131.260.090, C16.320.180.090
MeSH 单一 ID: D019280
进入的组:
  • Branchio Oto Renal Syndrome
  • Melnick-Fraser Syndrome
  • Melnick Fraser Syndrome
  • Branchio-Otorenal Syndrome
  • Branchiootorenal Dysplasia
  • Dysplasia, Branchiootorenal
  • BOR Syndrome
  • Branchio-Otorenal Dysplasia
  • Branchiootorenal Syndrome 2
  • Branchiootorenal Syndrome 1
  • Branchio-Oculo-Facial Syndrome
  • Branchio Oculo Facial Syndrome
  • Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging
  • Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome
  • Lip Pseudocleft Hemangiomatous Branchial Cyst Syndrome
  • Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome
  • Hemangiomatous Branchial Clefts Lip Pseudocleft Syndrome
  • Lee Root Fenske Syndrome
  • BOF Syndrome
  • Syndrome, BOF
  • Branchiooculofacial Syndrome
早前的内容:
  • Abnormalities, Multiple (1966-1996)
  • Chromosome Abnormalities (1966-1996)

留言 (0)

沒有登入
gif