Literature DB >> 10607954

Knobloch syndrome involving midline scalp defect of the frontal region.

L C Sniderman1, R K Koenekoop, A M O'Gorman, R H Usher, M R Sufrategui, B Moroz, G V Watters, V M Der Kaloustian.   

Abstract

We report on a 4-year-old boy with Knobloch syndrome. He has vitreoretinal degeneration, high myopia, cataract, telecanthus, hypertelorism, and a high-arched palate. He also has a defect of the anterior midline scalp with involvement of the frontal bone as documented by a computed tomography (CT) scan. The brain was normal on CT scan and magnetic resonance imaging. We present a review of the 23 published cases with this syndrome. Our patient illustrates the importance of investigating for underlying ocular and central nervous system pathology whenever midline scalp defects are present. Copyright 2000 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2000        PMID: 10607954

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  7 in total

1.  Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome.

Authors:  O T Suzuki; A L Sertié; V M Der Kaloustian; F Kok; M Carpenter; J Murray; A E Czeizel; S E Kliemann; S Rosemberg; M Monteiro; B R Olsen; M R Passos-Bueno
Journal:  Am J Hum Genet       Date:  2002-11-01       Impact factor: 11.025

Review 2.  Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutations.

Authors:  Ahmet Okay Caglayan; Jacob F Baranoski; Fesih Aktar; Wengi Han; Beyhan Tuysuz; Aslan Guzel; Bulent Guclu; Hande Kaymakcalan; Berrin Aktekin; Gozde Tugce Akgumus; Phillip B Murray; Emine Z Erson-Omay; Caner Caglar; Mehmet Bakircioglu; Yildirim Bayezit Sakalar; Ebru Guzel; Nihat Demir; Oguz Tuncer; Senem Senturk; Baris Ekici; Frank J Minja; Nenad Šestan; Katsuhito Yasuno; Kaya Bilguvar; Huseyin Caksen; Murat Gunel
Journal:  Pediatr Neurol       Date:  2014-09-04       Impact factor: 3.372

3.  Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemia.

Authors:  Vinit B Mahajan; Ann Haskins Olney; Penny Garrett; Ajit Chary; Ecaterina Dragan; Gary Lerner; Jeffrey Murray; Alexander G Bassuk
Journal:  Am J Med Genet A       Date:  2010-11       Impact factor: 2.802

Review 4.  Endostatin's emerging roles in angiogenesis, lymphangiogenesis, disease, and clinical applications.

Authors:  Amit Walia; Jessica F Yang; Yu-Hui Huang; Mark I Rosenblatt; Jin-Hong Chang; Dimitri T Azar
Journal:  Biochim Biophys Acta       Date:  2015-09-12

5.  The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development.

Authors:  Paul G Matteson; Jigar Desai; Ron Korstanje; Gloria Lazar; Tanya E Borsuk; Jarod Rollins; Sindhuja Kadambi; Jamie Joseph; Taslima Rahman; Jason Wink; Rym Benayed; Beverly Paigen; James H Millonig
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-04       Impact factor: 11.205

6.  Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome.

Authors:  Alireza Haghighi; Amit Tiwari; Niloofar Piri; Gudrun Nürnberg; Nasrollah Saleh-Gohari; Amirreza Haghighi; John Neidhardt; Peter Nürnberg; Wolfgang Berger
Journal:  PLoS One       Date:  2014-11-13       Impact factor: 3.240

7.  Novel pathogenic mutations and skin biopsy analysis in Knobloch syndrome.

Authors:  Oscar Suzuki; Erika Kague; Kelly Bagatini; Hongmin Tu; Ritva Heljasvaara; Lorenza Carvalhaes; Elisandra Gava; Gisele de Oliveira; Paulo Godoi; Glaucius Oliva; Gregory Kitten; Taina Pihlajaniemi; Maria-Rita Passos-Bueno
Journal:  Mol Vis       Date:  2009-04-23       Impact factor: 2.367

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.