Literature DB >> 12214284

The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.

Nazneen Rahman1, Melanie Dunstan, M Dawn Teare, Sandra Hanks, Sarah J Edkins, Jaime Hughes, Graham R Bignell, Grazia Mancini, Wim Kleijer, Mary Campbell, Gokhan Keser, Carol Black, Nigel Williams, Laura Arbour, Matthew Warman, Andrea Superti-Furga, P Andrew Futreal, F Michael Pope.   

Abstract

Juvenile hyaline fibromatosis (JHF) is an autosomal recessive condition characterized by multiple subcutaneous nodular tumors, gingival fibromatosis, flexion contractures of the joints, and an accumulation of hyaline in the dermis. We performed a genomewide linkage search in two families with JHF from the same region of the Indian state of Gujarat and identified a region of homozygosity on chromosome 4q21. Dense microsatellite analyses within this interval in five families with JHF who were from diverse origins demonstrate that all are compatible with linkage to chromosome 4q21 (multipoint LOD score 5.5). Meiotic recombinants place the gene for JHF within a 7-cM interval bounded by D4S2393 and D4S395.

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Year:  2002        PMID: 12214284      PMCID: PMC378553          DOI: 10.1086/342776

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  21 in total

1.  Selected case from the Arkadi M. Rywlin International Pathology Slide Seminar: hyaline fibromatosis.

Authors:  P W Allen
Journal:  Adv Anat Pathol       Date:  2001-05       Impact factor: 3.875

2.  Winchester syndrome. A case report and literature review.

Authors:  S Prapanpoch; R J Jorgenson; R P Langlais; P V Nummikoski
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1992-11

3.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

Review 4.  Two siblings with juvenile hyaline fibromatosis: case reports and review of the literature.

Authors:  G Keser; B Karabulut; F Oksel; C Calli; E E Ustün; T Akalin; H Koçanaoğullari; G Gümüdiş; E Doğanavşargil
Journal:  Clin Rheumatol       Date:  1999       Impact factor: 2.980

5.  Faster sequential genetic linkage computations.

Authors:  R W Cottingham; R M Idury; A A Schäffer
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

6.  Infantile systemic hyalinosis: newly recognized disorder of collagen?

Authors:  M T Glover; B D Lake; D J Atherton
Journal:  Pediatrics       Date:  1991-02       Impact factor: 7.124

7.  Systemic hyalinosis (juvenile hyaline fibromatosis). Ultrastructure of the hyaline with particular reference to the cross-banded structure.

Authors:  H Ishikawa; H Maeda; H Takamatsu; Y Saito
Journal:  Arch Dermatol Res       Date:  1979-06-25       Impact factor: 3.017

8.  Juvenile hyaline fibromatosis. A histologic and histochemical study.

Authors:  A Mayer-da-Silva; A Poiares-Baptista; F Guerra Rodrigo; M Teresa-Lopes
Journal:  Arch Pathol Lab Med       Date:  1988-09       Impact factor: 5.534

Review 9.  Infantile systemic hyalinosis in a black infant.

Authors:  E E Sahn; C F Salinas; M A Sens; J Key; F K Swiger; K A Holbrook
Journal:  Pediatr Dermatol       Date:  1994-03       Impact factor: 1.588

10.  Skin collagen defects in a patient with juvenile hyaline fibromatosis.

Authors:  B Lubec; I Steinert; F Breier; W Jurecka; K Pillwein; S Fang-Kircher
Journal:  Arch Dis Child       Date:  1995-09       Impact factor: 3.791

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  19 in total

1.  Juvenile hyaline fibromatosis: focus on radiographic features in adulthood.

Authors:  Samy Slimani; Assia Haddouche; Sabrina Haid; Aicha Ladjouze-Rezig
Journal:  Rheumatol Int       Date:  2010-07-27       Impact factor: 2.631

2.  Human genetic variation altering anthrax toxin sensitivity.

Authors:  Mikhail Martchenko; Sophie I Candille; Hua Tang; Stanley N Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-06       Impact factor: 11.205

3.  Infantile systemic hyalinosis: report of three Iranian children and review of the literature.

Authors:  Yahya Aghighi; Shahla Bahremand; Laleh Razavi Nematollahi
Journal:  Clin Rheumatol       Date:  2005-12-03       Impact factor: 2.980

4.  Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system.

Authors:  Rafael Denadai; Cassio E Raposo-Amaral; Débora Bertola; Chong Kim; Nivaldo Alonso; Thomas Hart; Sangwoo Han; Rafael F Stelini; Celso L Buzzo; Cesar A Raposo-Amaral; P Suzanne Hart
Journal:  Am J Med Genet A       Date:  2012-03-01       Impact factor: 2.802

Review 5.  The dark sides of capillary morphogenesis gene 2.

Authors:  Julie Deuquet; Ekkehart Lausch; Andrea Superti-Furga; F Gisou van der Goot
Journal:  EMBO J       Date:  2011-12-06       Impact factor: 11.598

6.  Clinical and imaging findings of systemic hyalinosis: two cases presenting with congenital arthrogryposis.

Authors:  So-Young Yoo; Ji Hye Kim; Ho Seok Kang; Yong Seung Hwang; Ki Joong Kim; In-One Kim; Jung-Eun Cheon; Su-Mi Shin; Chong Jai Kim; Jee Hun Lee; Mun Hyang Lee; Jong Hee Chae
Journal:  Skeletal Radiol       Date:  2010-02-06       Impact factor: 2.199

7.  Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis.

Authors:  Oonagh Dowling; Analisa Difeo; Maria C Ramirez; Turgut Tukel; Goutham Narla; Luisa Bonafe; Hulya Kayserili; Memnune Yuksel-Apak; Amy S Paller; Karen Norton; Ahmad S Teebi; Valerie Grum-Tokars; Gail S Martin; George E Davis; Marc J Glucksman; John A Martignetti
Journal:  Am J Hum Genet       Date:  2003-09-12       Impact factor: 11.025

8.  Infantile Systemic Hyalinosis: Novel Founder Mutation in the Initiation Codon among "Malis (Farmers)" in Jodhpur.

Authors:  Jai Prakash Soni; Ratna D Puri; Kapil Jetha; G S L Bhavani; Monika Chaudhary; Sudha Kohli; I C Verma
Journal:  Indian J Pediatr       Date:  2016-10-18       Impact factor: 1.967

9.  Juvenile Hyaline Fibromatosis Management With a Diode Laser: A Rare Case Report.

Authors:  Reza Fekrazad; Farzad Fazilat; Katayoun Am Kalhori; Neda Hakimiha; Mehrdad Amirmoini; Maryam Nikhalat Jahromi
Journal:  J Lasers Med Sci       Date:  2020-01-18

10.  Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

Authors:  Sandra Hanks; Sarah Adams; Jenny Douglas; Laura Arbour; David J Atherton; Sevim Balci; Harald Bode; Mary E Campbell; Murray Feingold; Gökhan Keser; Wim Kleijer; Grazia Mancini; John A McGrath; Francesco Muntoni; Arti Nanda; M Dawn Teare; Matthew Warman; F Michael Pope; Andrea Superti-Furga; P Andrew Futreal; Nazneen Rahman
Journal:  Am J Hum Genet       Date:  2003-08-21       Impact factor: 11.025

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