Achondrogenesis

Changed by Jeremy Jones, 7 Apr 2023
Disclosures - updated 6 Dec 2022: Nothing to disclose

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Achondrogenesis refers to a group of rare and extreme skeletal dysplasias.

Epidemiology

The estimated incidence is 1:40,000, with no recognised gender predilection.

Pathology

It is classified as an osteochondrodysplasia, meaning deficiency of both bone and cartilage development.

Subtypes

There are The condition has several recognised subtypes:

Genetics

Mutations in the SLC26A2 and COL2A1 genes cause achondrogenesis types 1B and 2, respectively. The genetic cause of achondrogenesis type 1A is still unknown. The patterns of inheritance are autosomal recessive in types 1A and 1B, and autosomal dominant with de-novo mutations in type B.

Radiographic features

Antenatal ultrasound

Sonographic diagnosis may be possible after 13 weeks of gestation, where nuchal oedema may be evident as an early (though non-specific) sign.

The fetal bony structures are often unable to be identified. There may also be extreme micromelia 5. Calvarial ossification may be preserved with the type II subtype which can, in turn, give a floating head appearance.

Additional sonographic findings include:

Other ancillary sonographic features that may be present include:

Treatment and prognosis

The prognosis is generally poor, with most infants being stillborn or dying soon after birth.

History and etymology

M FracaroAchondrogenesis was first described a case of achondrogenesisby Prof. Marco Fracaro (1926-2008) in 1952 although it was previously known as Parenti Fraccaro syndrome.

Differential diagnosis

General considerations for mild cases include hypochondrogenesis. For absent If there is calvarial bone(s) absence (type 1A/1B) on antenatal ultrasound, consider acrania.

See also

  • achondroplasia: a common cause of dwarfism; not to be confused with achondrogenesis

  • -<p><strong>Achondrogenesis</strong> refers to a group of rare and extreme <a href="/articles/skeletal-dysplasia">skeletal dysplasias</a>.</p><h4>Epidemiology</h4><p>The estimated incidence is 1:40,000 with no recognised gender predilection.</p><h4>Pathology</h4><p>It is classified as an <a href="/articles/osteochondrodysplasias">osteochondrodysplasia</a>, meaning deficiency of both bone and cartilage development. </p><h5>Subtypes</h5><p>There are several recognised subtypes:</p><ul>
  • +<p><strong>Achondrogenesis</strong> refers to a group of rare and extreme <a href="/articles/skeletal-dysplasia">skeletal dysplasias</a>.</p><h4>Epidemiology</h4><p>The estimated incidence is 1:40,000, with no recognised gender predilection.</p><h4>Pathology</h4><p>It is classified as an <a href="/articles/osteochondrodysplasias">osteochondrodysplasia</a>, meaning deficiency of both bone and cartilage development. The condition has several recognised subtypes:</p><ul>
  • -<strong>type 1</strong><ul>
  • -<li>
  • -<strong>type 1A:</strong> <a href="/articles/achondrogenesis-1a">Houston-Harris subtype</a>
  • -</li>
  • -<li>
  • -<strong>type 1B:</strong> <a href="/articles/achondrogenesis-1b">Parenti-Fraccaro subtype</a>
  • -</li>
  • +<p><strong>type 1</strong></p>
  • +<ul>
  • +<li><p><strong>type 1A</strong>: <a href="/articles/achondrogenesis-1a">Houston-Harris subtype</a></p></li>
  • +<li><p><strong>type 1B</strong>: <a href="/articles/achondrogenesis-1b">Parenti-Fraccaro subtype</a></p></li>
  • -<li>
  • -<strong>type 2:</strong> <a href="/articles/langer-saldino-syndrome">Langer-Saldino achondrogenesis</a>
  • -</li>
  • -</ul><h5>Genetics</h5><p>Mutations in the SLC26A2 and COL2A1 genes cause achondrogenesis types 1B and 2, respectively. The genetic cause of achondrogenesis type 1A is still unknown. The patterns of inheritance are autosomal recessive in types 1A and 1B, and autosomal dominant with de-novo mutations in type B.</p><h4>Radiographic features</h4><h5>Antenatal ultrasound</h5><p>Sonographic diagnosis may be possible after 13 weeks of gestation, where nuchal oedema may be evident as an early (though non-specific) sign.</p><p>The fetal bony structures are often unable to be identified. There may also be extreme <a href="/articles/micromelia">micromelia</a> <sup>5</sup>. Calvarial ossification may be preserved with the type II subtype which can, in turn, give a <a href="/articles/floating-head">floating head</a> appearance.</p><p>Additional sonographic findings include:</p><ul>
  • -<li><a href="/articles/micrognathia">micrognathia</a></li>
  • -<li><a href="/articles/macrocephaly">macrocephaly</a></li>
  • -<li><a href="/articles/frontal-bossing">frontal bossing</a></li>
  • -<li>flat face</li>
  • -<li>anteverted nares</li>
  • -<li><a href="/articles/long-philtrum">long philtrum</a></li>
  • -<li><a href="/articles/narrow-fetal-thorax">narrow fetal thorax</a></li>
  • -<li>
  • -<a href="/articles/pulmonary-aplasia">lung aplasia</a>/<a href="/articles/pulmonary-hypoplasia">hypoplasia</a>
  • -</li>
  • -<li>rib fractures may be present in type 1A</li>
  • +<li><p><strong>type 2</strong>: <a href="/articles/langer-saldino-syndrome">Langer-Saldino achondrogenesis</a></p></li>
  • +</ul><h5>Genetics</h5><p>Mutations in the SLC26A2 and COL2A1 genes cause achondrogenesis types 1B and 2, respectively. The genetic cause of achondrogenesis type 1A is still unknown. The patterns of inheritance are autosomal recessive in types 1A and 1B and autosomal dominant with de-novo mutations in type B.</p><h4>Radiographic features</h4><h5>Antenatal ultrasound</h5><p>Sonographic diagnosis may be possible after 13 weeks of gestation, where nuchal oedema may be evident as an early (though non-specific) sign.</p><p>The fetal bony structures are often unable to be identified. There may also be extreme <a href="/articles/micromelia">micromelia</a> <sup>5</sup>. Calvarial ossification may be preserved with the type II subtype which can, in turn, give a <a href="/articles/floating-head">floating head</a> appearance.</p><p>Additional sonographic findings include:</p><ul>
  • +<li><p><a href="/articles/micrognathia">micrognathia</a></p></li>
  • +<li><p><a href="/articles/macrocephaly">macrocephaly</a></p></li>
  • +<li><p><a href="/articles/frontal-bossing">frontal bossing</a></p></li>
  • +<li><p>flat face</p></li>
  • +<li><p>anteverted nares</p></li>
  • +<li><p><a href="/articles/long-philtrum">long philtrum</a></p></li>
  • +<li><p><a href="/articles/narrow-fetal-thorax">narrow fetal thorax</a></p></li>
  • +<li><p><a href="/articles/pulmonary-aplasia">lung aplasia</a>/<a href="/articles/pulmonary-hypoplasia">hypoplasia</a></p></li>
  • +<li><p>rib fractures may be present in type 1A</p></li>
  • -<li><a href="/articles/polyhydramnios">polyhydramnios</a></li>
  • -<li>development of <a href="/articles/hydrops-fetalis">hydrops fetalis</a>
  • -</li>
  • -</ul><h4>Treatment and prognosis</h4><p>The prognosis is generally poor, with most infants being stillborn or dying soon after birth.</p><h4>History and etymology</h4><p><strong>M Fracaro</strong> first described a case of achondrogenesis in 1952.</p><h4>Differential diagnosis</h4><p>General considerations for mild cases include <a href="/articles/hypochondrogenesis">hypochondrogenesis</a>. For absent calvarial bone(s) (type 1A/1B) on antenatal ultrasound, consider <a href="/articles/acrania">acrania</a>.</p><h4>See also</h4><ul><li>
  • -<a href="/articles/achondroplasia">achondroplasia</a>: a common cause of dwarfism; not to be confused with achondrogenesis</li></ul>
  • +<li><p><a href="/articles/polyhydramnios">polyhydramnios</a></p></li>
  • +<li><p>development of <a href="/articles/hydrops-fetalis">hydrops fetalis</a></p></li>
  • +</ul><h4>Treatment and prognosis</h4><p>The prognosis is generally poor, with most infants being stillborn or dying soon after birth.</p><h4>History and etymology</h4><p>Achondrogenesis was first described by <strong>Prof. Marco Fracaro</strong> (1926-2008) in 1952 although it was previously known as Parenti Fraccaro syndrome.</p><h4>Differential diagnosis</h4><p>General considerations for mild cases include <a href="/articles/hypochondrogenesis">hypochondrogenesis</a>. If there is calvarial bone absence (type 1A/1B) on antenatal ultrasound, consider <a href="/articles/acrania">acrania</a>.</p><h4>See also</h4><ul><li><p><a href="/articles/achondroplasia">achondroplasia</a>: a common cause of dwarfism; not to be confused with achondrogenesis</p></li></ul>

References changed:

  • 1. Taner M, Kurdoglu M, Taskiran C, Onan M, Gunaydin G, Himmetoglu O. Prenatal Diagnosis of Achondrogenesis Type I: A Case Report. Cases J. 2008;1(1):406. <a href="https://doi.org/10.1186/1757-1626-1-406">doi:10.1186/1757-1626-1-406</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/19094214">Pubmed</a>
  • 2. Superti-Furga A. Achondrogenesis Type 1B. J Med Genet. 1996;33(11):957-61. <a href="https://doi.org/10.1136/jmg.33.11.957">doi:10.1136/jmg.33.11.957</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/8950678">Pubmed</a>
  • 3. Jaeger H, Schmitz-Stolbrink A, Hulde J, Novak M, Roggenkamp K, Mathias K. The Boneless Neonate: A Severe Form of Achondrogenesis Type I. Pediatr Radiol. 1994;24(5):319-21. <a href="https://doi.org/10.1007/BF02012114">doi:10.1007/BF02012114</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/7824361">Pubmed</a>
  • 4. Freeze H. Achondrogenesis Type 1A--From Mouse to Human. N Engl J Med. 2010;362(3):266-7. <a href="https://doi.org/10.1056/NEJMe0911455">doi:10.1056/NEJMe0911455</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/20089978">Pubmed</a>
  • 5. Lee H, Doh J, Kim C, Chi J. Achondrogenesis Type II (Langer-Saldino Achondrogenesis): A Case Report. J Korean Med Sci. 2000;15(5):604-8. <a href="https://doi.org/10.3346/jkms.2000.15.5.604">doi:10.3346/jkms.2000.15.5.604</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/11069003">Pubmed</a>
  • 6. Kapur R. Achondrogenesis. Pediatr Dev Pathol. 2007;10(4):253-5. <a href="https://doi.org/10.2350/07-01-0216.1">doi:10.2350/07-01-0216.1</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/17638434">Pubmed</a>
  • 7. Aigner T, Rau T, Niederhagen M et al. Achondrogenesis Type IA (Houston-Harris): A Still-Unresolved Molecular Phenotype. Pediatr Dev Pathol. 2007;10(4):328-34. <a href="https://doi.org/10.2350/06-07-0134.1">doi:10.2350/06-07-0134.1</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/17638425">Pubmed</a>
  • 8. Tongsong T, Srisomboon J, Sudasna J. Prenatal Diagnosis of Langer-Saldino Achondrogenesis. J Clin Ultrasound. 1995;23(1):56-8. <a href="https://doi.org/10.1002/jcu.1870230112">doi:10.1002/jcu.1870230112</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/7699096">Pubmed</a>
  • 9. Reinhard Schumacher, Laurie H. Seaver, Jürgen Spranger. Fetal Radiology. (2010) ISBN: 9783642035593 - <a href="http://books.google.com/books?vid=ISBN9783642035593">Google Books</a>
  • 10. Whitley C & Gorlin R. Achondrogenesis: New Nosology with Evidence of Genetic Heterogeneity. Radiology. 1983;148(3):693-8. <a href="https://doi.org/10.1148/radiology.148.3.6878687">doi:10.1148/radiology.148.3.6878687</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/6878687">Pubmed</a>
  • 11. Michael Entezami, Ursula Knoll, Matthias Albig et al. Ultrasound Diagnosis of Fetal Anomalies. (2004) ISBN: 9781588902122 - <a href="http://books.google.com/books?vid=ISBN9781588902122">Google Books</a>
  • 1. Taner MZ, Kurdoglu M, Taskiran C et-al. Prenatal diagnosis of achondrogenesis type I: a case report. Cases J. 2008;1 (1): 406. <a href="http://dx.doi.org/10.1186/1757-1626-1-406">doi:10.1186/1757-1626-1-406</a> - <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615762">Free text at pubmed</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/19094214">Pubmed citation</a><div class="ref_v2"></div>
  • 2. Superti-furga A. Achondrogenesis type 1B. J. Med. Genet. 1996;33 (11): 957-61. <a href="http://jmg.bmj.com/cgi/pmidlookup?view=long&pmid=8950678">J. Med. Genet. (link)</a> - <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1050792">Free text at pubmed</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/8950678">Pubmed citation</a><div class="ref_v2"></div>
  • 3. Jaeger HJ, Schmitz-stolbrink A, Hulde J et-al. The boneless neonate: a severe form of achondrogenesis type I. Pediatr Radiol. 1994;24 (5): 319-21. - <a href="http://www.ncbi.nlm.nih.gov/pubmed/7824361">Pubmed citation</a><div class="ref_v2"></div>
  • 4. Freeze HH. Achondrogenesis type 1A--from mouse to human. N. Engl. J. Med. 2010;362 (3): 266-7. <a href="http://dx.doi.org/10.1056/NEJMe0911455">doi:10.1056/NEJMe0911455</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/20089978">Pubmed citation</a><div class="ref_v2"></div>
  • 5. Lee HS, Doh JW, Kim CJ et-al. Achondrogenesis type II (Langer-Saldino achondrogenesis): a case report. J. Korean Med. Sci. 2000;15 (5): 604-8. <a href="http://jkms.org/DOIx.php?id=10.3346/jkms.2000.15.5.604">J. Korean Med. Sci. (link)</a> - <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054684">Free text at pubmed</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/11069003">Pubmed citation</a><div class="ref_v2"></div>
  • 6. Kapur RP. Achondrogenesis. Pediatr. Dev. Pathol. 10 (4): 253-5. <a href="http://dx.doi.org/10.2350/07-01-0216.1">doi:10.2350/07-01-0216.1</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/17638434">Pubmed citation</a><div class="ref_v2"></div>
  • 7. Aigner T, Rau T, Niederhagen M et-al. Achondrogenesis Type IA (Houston-Harris): a still-unresolved molecular phenotype. Pediatr. Dev. Pathol. 10 (4): 328-34. <a href="http://dx.doi.org/10.2350/06-07-0134.1">doi:10.2350/06-07-0134.1</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/17638425">Pubmed citation</a><div class="ref_v2"></div>
  • 8. Tongsong T, Srisomboon J, Sudasna J. Prenatal diagnosis of Langer-Saldino achondrogenesis. J Clin Ultrasound. 1995;23 (1): 56-8. - <a href="http://www.ncbi.nlm.nih.gov/pubmed/7699096">Pubmed citation</a><div class="ref_v2"></div>
  • 9. Schumacher R, Seaver LH, Spranger J. Fetal Radiology, A Diagnostic Atlas. Springer Verlag. (2011) ISBN:3642035590. <a href="http://books.google.com/books?vid=ISBN3642035590">Read it at Google Books</a> - <a href="http://www.amazon.com/gp/product/3642035590?ie=UTF8&tag=radiopaediaor-20&linkCode=as2&camp=1789&creative=9325&creativeASIN=3642035590">Find it at Amazon</a><div class="ref_v2"></div>
  • 10. Whitley CB, Gorlin RJ. Achondrogenesis: new nosology with evidence of genetic heterogeneity. Radiology. 1983;148 (3): 693-8. <a href="http://radiology.rsna.org/content/148/3/693.abstract">Radiology (abstract)</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/6878687">Pubmed citation</a><div class="ref_v2"></div>
  • 11. Entezami M, Albig M, Knoll U et-al. Ultrasound Diagnosis of Fetal Anomalies. Thieme. (2003) ISBN:1588902129. <a href="http://books.google.com/books?vid=ISBN1588902129">Read it at Google Books</a> - <a href="http://www.amazon.com/gp/product/1588902129?ie=UTF8&tag=radiopaediaor-20&linkCode=as2&camp=1789&creative=9325&creativeASIN=1588902129">Find it at Amazon</a><div class="ref_v2"></div>

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Parenti Fraccaro syndrome
Slug was set to parenti-fraccaro-syndrome-1.
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