TITLE

Autosomal dominant congenital Horner's syndrome in a Dutch family

AUTHOR(S)
Hageman, G; Ippel, P F; te Nijenhuis, F C
PUB. DATE
January 1992
SOURCE
Journal of Neurology, Neurosurgery & Psychiatry;Jan1992, Vol. 55 Issue 1, p28
SOURCE TYPE
Academic Journal
DOC. TYPE
journal article
ABSTRACT
No abstract available.
ACCESSION #
66052736

 

Related Articles

  • Popliteal Pterygium Syndrome: A Rare Entity. Qasim, Muhammad; Shaukat, Mahmood // APSP Journal of Case Reports;2012, Vol. 3 Issue 1, p1 

    The popliteal pterygium syndrome is a congenital malformation that includes orofacial, musculoskeletal and genitourinary anomalies. It is a rare autosomal dominant disorder. We report one family with popliteal pterygium syndrome affecting father and his two daughters, who underwent surgical...

  • Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract. Ma, Z.; Zheng, J.; Yang, F.; Ji, J.; Li, X.; Tang, X.; Yuan, X.; Zhang, X.; Sun, H. // British Journal of Ophthalmology;Nov2005, Vol. 89 Issue 11, p1535 

    Presents a letter to the editor about mutation of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract.

  • Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations. Forshew, Tim; Johnson, Colin A.; Khaliq, Shagufta; Pasha, Shanaz; Willis, Catherine; Abbasi, Rashida; Tee, Louise; Smith, Ursula; Trembath, Richard C.; Mehdi, Syed Qasim; Moore, Anthony T.; Maher, Eamonn R. // Human Genetics;Sep2005, Vol. 117 Issue 5, p452 

    Isolated (non-syndromic) congenital cataract may be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive trait. Considerable progress has been made in identifying genes and loci for dominantly inherited cataract, but the molecular basis for autosomal recessive disease...

  • Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant condition. Martin, Donna M.; Gorski, Jerome L. // Journal of Medical Genetics;Aug2001, Vol. 38 Issue 8, p547 

    Reports that microphthalmia and related ocular abnormalities are a common component of many multiple congenital anomaly syndromes. Case discussions; Autosomal dominant conditions.

  • familial adenomatous polyposis.  // Taber's Cyclopedic Medical Dictionary (2009);2009, Issue 21, p846 

    An encyclopedia entry for "familial adenomatous polyposis," which refers to a rare autosomal dominant syndrome, is presented.

  • Poikiloderma a varied presentation - Huriez syndrome. Kharge, Priyadarshini; Fernendes, Carol; Jairath, Vijayeeta; Mohan, Madan; Chandra, Suresh // Indian Dermatology Online Journal;Jan/Feb2015, Vol. 6 Issue 1, p27 

    Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.

  • Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndrome. Goodship, J. A.; O'Sullivan, J.; Chinnery, P. F.; Ryan, A. K.; Ziakas, N.; Hall, C. M.; Clarke, M. // Journal of Medical Genetics;Mar2002, Vol. 39 Issue 3, p221 

    Presents a letter to the editor about an autosomal dominant syndrome.

  • Heredity in Large Vestibular Aqueduct Syndrome. Joachims, Zoha; Joachims, Henry Z.; Golz, Avishai; Hefer, Tsila; Finnell, Richard H. // Journal of Otolaryngology;Jul/Aug2000, Vol. 29 Issue 4, p244 

    Presents a case report on a family whose members suffer from the large vestibular aqueduct (VA) syndrome. Diagnosis of normal hearing in both parents and hearing loss in children; Clinical and radiographic features of a congenital malformation characterized by a VA; Occurrence of anomaly due to...

  • A unique form of autosomal dominant cataract explained by gene conversion between β-crystallin B2 and its pseudogene. Vanita; Sarhadi, Virinder; Reis, André; Jung, Martin; Singh, Daljit; Sperling, Karl; Singh, Jai Rup; Bürger, Joachim // Journal of Medical Genetics;Jun2001, Vol. 38 Issue 6, p392 

    Presents a letter to the editor about autosomal dominant congenital cataract.

  • Horner's syndrome secondary to asymptomatic pneumothorax in an adolescent. Mutalib, Mohamed; Vandervelde, Clive; Varghese, Ajay; Sallomi, David F.; De Silva, Padmani; Casey, J. M. Hickman; Howlett, David C.; Hickman Casey, J M // European Journal of Pediatrics;May2007, Vol. 166 Issue 5, p507 

    Horner's syndrome is uncommon in the paediatric population, but is seen more in infancy, and most cases are either congenital or related to birth trauma, head and neck tumours or thoracic surgery. We report an unusual cause of Horner's syndrome in a healthy adolescent boy secondary to a large,...

Share

Read the Article

Courtesy of THE LIBRARY OF VIRGINIA

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics