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Nosology and Classification of Genetic Skeletal Disorders: 2010 Revision

Identifieur interne : 002082 ( Pmc/Curation ); précédent : 002081; suivant : 002083

Nosology and Classification of Genetic Skeletal Disorders: 2010 Revision

Auteurs : Matthew L. Warman [États-Unis] ; Valerie Cormier-Daire [France] ; Christine Hall [Royaume-Uni] ; Deborah Krakow [États-Unis] ; Ralph Lachman [États-Unis] ; Martine Lemerrer [France] ; Geert Mortier [Belgique] ; Stefan Mundlos [Allemagne] ; Gen Nishimura [Japon] ; David L. Rimoin [États-Unis] ; Stephen Robertson [Nouvelle-Zélande] ; Ravi Savarirayan [Australie] ; David Sillence [Australie] ; Juergen Spranger [Allemagne] ; Sheila Unger [Allemagne, Suisse] ; Bernhard Zabel [Allemagne] ; Andrea Superti-Furga [Allemagne, Suisse]

Source :

RBID : PMC:3166781

Abstract

Genetic disorders involving the skeletal system arise through disturbances in the complex processes of skeletal development, growth and homeostasis and remain a diagnostic challenge because of their variety. The Nosology and Classification of Genetic Skeletal Disorders provides an overview of recognized diagnostic entities and groups them by clinical and radiographic features and molecular pathogenesis. The aim is to provide the Genetics, Pediatrics and Radiology community with a list of recognized genetic skeletal disorders that can be of help in the diagnosis of individual cases, in the delineation of novel disorders, and in building bridges between clinicians and scientists interested in skeletal biology. In the 2010 revision, 456 conditions were included and placed in 40 groups defined by molecular, biochemical, and/or radiographic criteria. Of these conditions, 316 were associated with mutations in one or more of 226 different genes, ranging from common, recurrent mutations to “private” found in single families or individuals. Thus, the Nosology is a hybrid between a list of clinically defined disorders, waiting for molecular clarification, and an annotated database documenting the phenotypic spectrum produced by mutations in a given gene. The Nosology should be useful for the diagnosis of patients with genetic skeletal diseases, particularly in view of the information flood expected with the novel sequencing technologies; in the delineation of clinical entities and novel disorders, by providing an overview of established nosologic entities; and for scientists looking for the clinical correlates of genes, proteins and pathways involved in skeletal biology. © 2011 Wiley-Liss, Inc.


Url:
DOI: 10.1002/ajmg.a.33909
PubMed: 21438135
PubMed Central: 3166781

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Le document en format XML

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<p>Genetic disorders involving the skeletal system arise through disturbances in the complex processes of skeletal development, growth and homeostasis and remain a diagnostic challenge because of their variety. The Nosology and Classification of Genetic Skeletal Disorders provides an overview of recognized diagnostic entities and groups them by clinical and radiographic features and molecular pathogenesis. The aim is to provide the Genetics, Pediatrics and Radiology community with a list of recognized genetic skeletal disorders that can be of help in the diagnosis of individual cases, in the delineation of novel disorders, and in building bridges between clinicians and scientists interested in skeletal biology. In the 2010 revision, 456 conditions were included and placed in 40 groups defined by molecular, biochemical, and/or radiographic criteria. Of these conditions, 316 were associated with mutations in one or more of 226 different genes, ranging from common, recurrent mutations to “private” found in single families or individuals. Thus, the Nosology is a hybrid between a list of clinically defined disorders, waiting for molecular clarification, and an annotated database documenting the phenotypic spectrum produced by mutations in a given gene. The Nosology should be useful for the diagnosis of patients with genetic skeletal diseases, particularly in view of the information flood expected with the novel sequencing technologies; in the delineation of clinical entities and novel disorders, by providing an overview of established nosologic entities; and for scientists looking for the clinical correlates of genes, proteins and pathways involved in skeletal biology. © 2011 Wiley-Liss, Inc.</p>
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<journal-id journal-id-type="iso-abbrev">Am. J. Med. Genet. A</journal-id>
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<article-title>Nosology and Classification of Genetic Skeletal Disorders: 2010 Revision</article-title>
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<name>
<surname>Warman</surname>
<given-names>Matthew L</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
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<name>
<surname>Cormier-Daire</surname>
<given-names>Valerie</given-names>
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<xref ref-type="aff" rid="au2">2</xref>
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<contrib contrib-type="author">
<name>
<surname>Hall</surname>
<given-names>Christine</given-names>
</name>
<xref ref-type="aff" rid="au3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Krakow</surname>
<given-names>Deborah</given-names>
</name>
<xref ref-type="aff" rid="au4">4</xref>
<xref ref-type="aff" rid="au5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lachman</surname>
<given-names>Ralph</given-names>
</name>
<xref ref-type="aff" rid="au4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>LeMerrer</surname>
<given-names>Martine</given-names>
</name>
<xref ref-type="aff" rid="au2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mortier</surname>
<given-names>Geert</given-names>
</name>
<xref ref-type="aff" rid="au6">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mundlos</surname>
<given-names>Stefan</given-names>
</name>
<xref ref-type="aff" rid="au7">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nishimura</surname>
<given-names>Gen</given-names>
</name>
<xref ref-type="aff" rid="au8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rimoin</surname>
<given-names>David L</given-names>
</name>
<xref ref-type="aff" rid="au4">4</xref>
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<contrib contrib-type="author">
<name>
<surname>Robertson</surname>
<given-names>Stephen</given-names>
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<xref ref-type="aff" rid="au9">9</xref>
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<name>
<surname>Savarirayan</surname>
<given-names>Ravi</given-names>
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<xref ref-type="aff" rid="au10">10</xref>
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<surname>Sillence</surname>
<given-names>David</given-names>
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<xref ref-type="aff" rid="au11">11</xref>
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<name>
<surname>Spranger</surname>
<given-names>Juergen</given-names>
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<xref ref-type="aff" rid="au12">12</xref>
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<name>
<surname>Unger</surname>
<given-names>Sheila</given-names>
</name>
<xref ref-type="aff" rid="au12">12</xref>
<xref ref-type="aff" rid="au13">13</xref>
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<contrib contrib-type="author">
<name>
<surname>Zabel</surname>
<given-names>Bernhard</given-names>
</name>
<xref ref-type="aff" rid="au12">12</xref>
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<contrib contrib-type="author">
<name>
<surname>Superti-Furga</surname>
<given-names>Andrea</given-names>
</name>
<xref ref-type="aff" rid="au12">12</xref>
<xref ref-type="aff" rid="au14">14</xref>
<xref ref-type="corresp" rid="cor1">*</xref>
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<aff id="au1">
<label>1</label>
<institution>Orthopaedic Research Laboratories, Department of Orthopaedic Surgery, The Howard Hughes Medical Institute, Children's Hospital</institution>
<addr-line>Boston, Massachusetts</addr-line>
</aff>
<aff id="au2">
<label>2</label>
<institution>Department of Genetics and INSERM U781, Paris Descartes University, Hôpital Necker Enfants Malades</institution>
<addr-line>Paris, France</addr-line>
</aff>
<aff id="au3">
<label>3</label>
<institution>Institute of Child Health, University of London</institution>
<addr-line>London, UK</addr-line>
</aff>
<aff id="au4">
<label>4</label>
<institution>Medical Genetics Institute, Steven Spielberg Building, Cedars-Sinai Medical Center</institution>
<addr-line>Los Angeles, California</addr-line>
</aff>
<aff id="au5">
<label>5</label>
<institution>Departments of Orthopaedic Surgery and Human Genetics, UCLA</institution>
<addr-line>Los Angeles, California</addr-line>
</aff>
<aff id="au6">
<label>6</label>
<institution>Department of Medical Genetics, University Hospital of Antwerp, University of Antwerp</institution>
<addr-line>Edegem, Belgium</addr-line>
</aff>
<aff id="au7">
<label>7</label>
<institution>Institut für Medizinische Genetik, Charité Universitätsmedizin Berlin, Max-Planck-Institut für Molekulare Genetik</institution>
<addr-line>Berlin, Germany</addr-line>
</aff>
<aff id="au8">
<label>8</label>
<institution>Department of Pediatric Imaging, Tokyo Metropolitan Children's Medical Center</institution>
<addr-line>Fuchu, Tokyo, Japan</addr-line>
</aff>
<aff id="au9">
<label>9</label>
<institution>Department of Paediatrics and Child Health, Dunedin School of Medicine, Otago University</institution>
<addr-line>Dunedin, New Zealand</addr-line>
</aff>
<aff id="au10">
<label>10</label>
<institution>Murdoch Children's Research Institute, Royal Children's Hospital, Department of Paediatrics, University of Melbourne</institution>
<addr-line>Victoria, Australia</addr-line>
</aff>
<aff id="au11">
<label>11</label>
<institution>Discipline of Genetic Medicine, The Children's Hospital at Westmead Clinical School, The University of Sydney</institution>
<addr-line>Westmead, Australia</addr-line>
</aff>
<aff id="au12">
<label>12</label>
<institution>Centre for Pediatrics and Adolescent Medicine, Freiburg University Hospital, University of Freiburg</institution>
<addr-line>Freiburg, Germany</addr-line>
</aff>
<aff id="au13">
<label>13</label>
<institution>Medical Genetics Service, University of Lausanne, CHUV—Centre Hospitalier Universitaire Vaudois</institution>
<addr-line>Lausanne, Switzerland</addr-line>
</aff>
<aff id="au14">
<label>14</label>
<institution>Department of Pediatrics, University of Lausanne, CHUV—Centre Hospitalier Universitaire Vaudois</institution>
<addr-line>Lausanne, Switzerland</addr-line>
</aff>
</contrib-group>
<author-notes>
<corresp id="cor1">*Correspondence to: Andrea Superti-Furga, Centre Hospitalier Universitaire Vaudois (CHUV), Av. Decker, 2, 1011 Lausanne, Switzerland. E-mail:
<email>asuperti@unil.ch</email>
</corresp>
<fn>
<p>The 9th ISDS meeting and the Nosology workshop were held in Boston in July 2009 and supported by The Manton Center for Orphan Disease Research, Children's Hospital, Boston, Massachusetts; Children's Orthopaedic Surgery Foundation, Inc., Boston, Massachusetts; The Osteogenesis Imperfecta Foundation, Gaithersburg, Maryland; Biomarin, Novato, California; and Enobia Pharma, Montreal, Quebec, Canada. The
<italic>2010 Nosology tables</italic>
are available online at the International Skeletal Dysplasia Society web site (
<ext-link ext-link-type="uri" xlink:href="http://www.isds.ch">http://www.isds.ch</ext-link>
).</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<month>5</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="epub">
<day>15</day>
<month>3</month>
<year>2011</year>
</pub-date>
<volume>155</volume>
<issue>5</issue>
<fpage>943</fpage>
<lpage>968</lpage>
<history>
<date date-type="received">
<day>16</day>
<month>12</month>
<year>2010</year>
</date>
<date date-type="accepted">
<day>30</day>
<month>12</month>
<year>2010</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2011 Wiley-Liss, Inc.</copyright-statement>
<copyright-year>2011</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.5/">
<license-p>Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.</license-p>
</license>
</permissions>
<abstract>
<p>Genetic disorders involving the skeletal system arise through disturbances in the complex processes of skeletal development, growth and homeostasis and remain a diagnostic challenge because of their variety. The Nosology and Classification of Genetic Skeletal Disorders provides an overview of recognized diagnostic entities and groups them by clinical and radiographic features and molecular pathogenesis. The aim is to provide the Genetics, Pediatrics and Radiology community with a list of recognized genetic skeletal disorders that can be of help in the diagnosis of individual cases, in the delineation of novel disorders, and in building bridges between clinicians and scientists interested in skeletal biology. In the 2010 revision, 456 conditions were included and placed in 40 groups defined by molecular, biochemical, and/or radiographic criteria. Of these conditions, 316 were associated with mutations in one or more of 226 different genes, ranging from common, recurrent mutations to “private” found in single families or individuals. Thus, the Nosology is a hybrid between a list of clinically defined disorders, waiting for molecular clarification, and an annotated database documenting the phenotypic spectrum produced by mutations in a given gene. The Nosology should be useful for the diagnosis of patients with genetic skeletal diseases, particularly in view of the information flood expected with the novel sequencing technologies; in the delineation of clinical entities and novel disorders, by providing an overview of established nosologic entities; and for scientists looking for the clinical correlates of genes, proteins and pathways involved in skeletal biology. © 2011 Wiley-Liss, Inc.</p>
</abstract>
<kwd-group>
<kwd>skeletal genetics</kwd>
<kwd>osteochondrodysplasias</kwd>
<kwd>nosology</kwd>
<kwd>dysostoses</kwd>
<kwd>molecular basis of disease</kwd>
</kwd-group>
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</front>
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