Literature DB >> 18492087

Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family study.

F Laccone1, M C Hannibal, J Neesen, W Grisold, P F Chance, H Rehder.   

Abstract

We report a family in which two siblings presented with an apparent dysmorphic syndrome, including hypotelorism, blepharophimosis, slight ptosis, epicanthal folds, microstomia and dysmorphic ears. One sibling had a cleft palate. Initially, blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) was suspected; however, mutation of the FOXL2 gene was not detected. Moreover, the patients' father and paternal grandmother had experienced recurrent episodes of unilateral brachial neuritis and were diagnosed to have hereditary neuralgic amyotrophy (HNA). HNA is a rare, inherited form of brachial neuritis whose phenotypic spectrum may include hypotelorism, cleft palate and other minor dysmorphisms. HNA maps to chromosome 17q25 and is associated with mutations in the SEPT9 gene. After confirming a heterozygous SEPT9 mutation (R88W) in the father and his mother, it became apparent that the dysmorphic features in the children were part of HNA and that previous complaints of the daughter, erroneously diagnosed as pronatio dolorosa and then epiphysiolysis of the capitellum humeri, were in fact a first neuralgic pain attack. Both children were shown to have inherited the paternal SEPT9 mutation. Wider recognition of HNA as a syndromic disorder may facilitate its diagnosis in affected young persons who may not yet have manifested episodes of brachial neuritis.

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Year:  2008        PMID: 18492087     DOI: 10.1111/j.1399-0004.2008.01022.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

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Authors:  Kurt Reynolds; Shuwen Zhang; Bo Sun; Michael A Garland; Yu Ji; Chengji J Zhou
Journal:  Birth Defects Res       Date:  2020-07-15       Impact factor: 2.344

Review 2.  Clinical and pathophysiological concepts of neuralgic amyotrophy.

Authors:  Nens van Alfen
Journal:  Nat Rev Neurol       Date:  2011-05-10       Impact factor: 42.937

3.  Identification of copy number variants associated with BPES-like phenotypes.

Authors:  Antoinet C J Gijsbers; Barbara D'haene; Yvonne Hilhorst-Hofstee; Marcel Mannens; Beate Albrecht; Joerg Seidel; David R Witt; Melissa K Maisenbacher; Bart Loeys; Ton van Essen; Egbert Bakker; Raoul Hennekam; Martijn H Breuning; Elfride De Baere; Claudia A L Ruivenkamp
Journal:  Hum Genet       Date:  2008-10-25       Impact factor: 4.132

4.  SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.

Authors:  M C Hannibal; E K Ruzzo; L R Miller; B Betz; J G Buchan; D M Knutzen; K Barnett; M L Landsverk; A Brice; E LeGuern; H M Bedford; B B Worrall; S Lovitt; S H Appel; E Andermann; T D Bird; P F Chance
Journal:  Neurology       Date:  2009-05-19       Impact factor: 9.910

5.  Pediatric Hereditary Neuralgic Amyotrophy: Successful Treatment With Intravenous Immunoglobulin and Insights Into SEPT9 Pathogenesis.

Authors:  Raymond Chuk; Megan Sheppard; Geoff Wallace; David Coman
Journal:  Child Neurol Open       Date:  2016-09-19

6.  A rare cause of brachial plexopathy: hereditary neuralgic amyotrophy.

Authors:  Hepsen Mine Serin; Sanem Yılmaz; Seda Kanmaz; Erdem Şimşek; Gül Aktan; Hasan Tekgül; Sarenur Gökben
Journal:  Turk Pediatri Ars       Date:  2019-09-25

7.  Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study.

Authors:  Katharina Neubauer; Doris Boeckelmann; Udo Koehler; Julia Kracht; Janbernd Kirschner; Manuela Pendziwiat; Barbara Zieger
Journal:  Cytoskeleton (Hoboken)       Date:  2018-10-10
  7 in total

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