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Erschienen in: Pediatric Radiology 4/2016

11.02.2016 | Original Article

Criteria for radiologic diagnosis of hypochondroplasia in neonates

verfasst von: Tomoko Saito, Keisuke Nagasaki, Gen Nishimura, Masaki Wada, Hiromi Nyuzuki, Masaki Takagi, Tomonobu Hasegawa, Naoko Amano, Jun Murotsuki, Hideaki Sawai, Takahiro Yamada, Shuhei Sato, Akihiko Saitoh

Erschienen in: Pediatric Radiology | Ausgabe 4/2016

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Abstract

Background

A radiologic diagnosis of hypochondroplasia is hampered by the absence of age-dependent radiologic criteria, particularly in the neonatal period.

Objective

To establish radiologic criteria and scoring system for identifying neonates with fibroblast growth factor receptor 3 (FGFR3)-associated hypochondroplasia.

Materials and methods

This retrospective study included 7 hypochondroplastic neonates and 30 controls. All subjects underwent radiologic examination within 28 days after birth. We evaluated parameters reflecting the presence of (1) short ilia, (2) squared ilia, (3) short greater sciatic notch, (4) horizontal acetabula, (5) short femora, (6) broad femora, (7) metaphyseal flaring, (8) lumbosacral interpedicular distance narrowing and (9) ovoid radiolucency of the proximal femora.

Results

Only parameters 1, 3, 4, 5 and 6 were statistically different between the two groups. Parameters 3, 5 and 6 did not overlap between the groups, while parameters 1 and 4 did. Based on these results, we propose a scoring system for hypochondroplasia. Two major criteria (parameters 3 and 6) were assigned scores of 2, whereas 4 minor criteria (parameters 1, 4, 5 and 9) were assigned scores of 1. All neonates with hypochondroplasia in our material scored ≥6.

Conclusion

Our set of diagnostic radiologic criteria might be useful for early identification of hypochondroplastic neonates.
Literatur
1.
Zurück zum Zitat Hicks J (2003) Achondroplasia family of skeletal dysplasia. In: The National Organization for Rare Disorders. Inc., editors. NORD guide to rare disorders. Lippincott Williams & Wilkins, Philadelphia, p 144 Hicks J (2003) Achondroplasia family of skeletal dysplasia. In: The National Organization for Rare Disorders. Inc., editors. NORD guide to rare disorders. Lippincott Williams & Wilkins, Philadelphia, p 144
2.
Zurück zum Zitat Hall BD, Spranger J (1979) Hypochondroplasia: clinical and radiological aspects in 39 cases. Radiology 133:95–100CrossRefPubMed Hall BD, Spranger J (1979) Hypochondroplasia: clinical and radiological aspects in 39 cases. Radiology 133:95–100CrossRefPubMed
3.
Zurück zum Zitat Matsui Y, Yasui N, Kimura T et al (1998) Genotype phenotype correlation in achondroplasia and hypochondroplasia. J Bone Joint Surg (Br) 80:1052–1056CrossRef Matsui Y, Yasui N, Kimura T et al (1998) Genotype phenotype correlation in achondroplasia and hypochondroplasia. J Bone Joint Surg (Br) 80:1052–1056CrossRef
4.
Zurück zum Zitat Appan S, Laurent S, Chapman M et al (1990) Growth and growth hormone therapy in hypochondroplasia. Acta Paediatr Scand 79:796–803CrossRefPubMed Appan S, Laurent S, Chapman M et al (1990) Growth and growth hormone therapy in hypochondroplasia. Acta Paediatr Scand 79:796–803CrossRefPubMed
5.
Zurück zum Zitat Saito T, Nagasaki K, Nishimura G et al (2012) Radiological clues to the early diagnosis of hypochondroplasia in the neonatal period: report of two patients. Am J Med Genet A 158A:630–634CrossRefPubMed Saito T, Nagasaki K, Nishimura G et al (2012) Radiological clues to the early diagnosis of hypochondroplasia in the neonatal period: report of two patients. Am J Med Genet A 158A:630–634CrossRefPubMed
6.
Zurück zum Zitat Bonnefoy O, Delbosc JM, Maugey-Laulom B et al (2006) Prenatal diagnosis of hypochondroplasia: three-dimensional multislice computed tomography findings and molecular analysis. Fetal Diagn Ther 21:18–217CrossRefPubMed Bonnefoy O, Delbosc JM, Maugey-Laulom B et al (2006) Prenatal diagnosis of hypochondroplasia: three-dimensional multislice computed tomography findings and molecular analysis. Fetal Diagn Ther 21:18–217CrossRefPubMed
7.
Zurück zum Zitat Huggins MJ, Mernagh JR, Steele L et al (1999) Prenatal sonographic diagnosis of hypochondroplasia in a high-risk fetus. Am J Med Genet 87:226–229CrossRefPubMed Huggins MJ, Mernagh JR, Steele L et al (1999) Prenatal sonographic diagnosis of hypochondroplasia in a high-risk fetus. Am J Med Genet 87:226–229CrossRefPubMed
8.
Zurück zum Zitat Jones SM, Robinson LK, Sperrazza R (1990) Prenatal diagnosis of skeletal dysplasia identified postnatally as hypochondroplasia. Am J Med Genet 36:404–407CrossRefPubMed Jones SM, Robinson LK, Sperrazza R (1990) Prenatal diagnosis of skeletal dysplasia identified postnatally as hypochondroplasia. Am J Med Genet 36:404–407CrossRefPubMed
9.
Zurück zum Zitat Karadimas C, Sifakis S, Valsamopoulos P et al (2006) Prenatal diagnosis of hypochondroplasia: report of two cases. Am J Med Genet A 140:998–1003CrossRefPubMed Karadimas C, Sifakis S, Valsamopoulos P et al (2006) Prenatal diagnosis of hypochondroplasia: report of two cases. Am J Med Genet A 140:998–1003CrossRefPubMed
10.
Zurück zum Zitat Kataoka S, Sawai H, Yamada H et al (2004) Radiographic and genetic diagnosis of sporadic hypochondroplasia early in the neonatal period. Prenat Diagn 24:45–49CrossRefPubMed Kataoka S, Sawai H, Yamada H et al (2004) Radiographic and genetic diagnosis of sporadic hypochondroplasia early in the neonatal period. Prenat Diagn 24:45–49CrossRefPubMed
11.
Zurück zum Zitat Lemyre E, Azouz EM, Teebi AS et al (1999) Bone dysplasia series. Achondroplasia, hypochondroplasia and thanatophoric dysplasia: review and update. Can Assoc Radiol J 50:185–197PubMed Lemyre E, Azouz EM, Teebi AS et al (1999) Bone dysplasia series. Achondroplasia, hypochondroplasia and thanatophoric dysplasia: review and update. Can Assoc Radiol J 50:185–197PubMed
12.
Zurück zum Zitat Xue Y, Sun A, Mekikian PB (2014) FGFR3 mutation frequency in 324 cases from the International Skeletal Dysplasia Registry. Mol Genet Genomic Med 2:497–503 Xue Y, Sun A, Mekikian PB (2014) FGFR3 mutation frequency in 324 cases from the International Skeletal Dysplasia Registry. Mol Genet Genomic Med 2:497–503
13.
Zurück zum Zitat Le Merrer M, Maroteaux P (1991) Cartilage hair hypoplasia in infancy: a misleading chondrodysplasia. Eur J Pediatr 150:847–851CrossRefPubMed Le Merrer M, Maroteaux P (1991) Cartilage hair hypoplasia in infancy: a misleading chondrodysplasia. Eur J Pediatr 150:847–851CrossRefPubMed
Metadaten
Titel
Criteria for radiologic diagnosis of hypochondroplasia in neonates
verfasst von
Tomoko Saito
Keisuke Nagasaki
Gen Nishimura
Masaki Wada
Hiromi Nyuzuki
Masaki Takagi
Tomonobu Hasegawa
Naoko Amano
Jun Murotsuki
Hideaki Sawai
Takahiro Yamada
Shuhei Sato
Akihiko Saitoh
Publikationsdatum
11.02.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Radiology / Ausgabe 4/2016
Print ISSN: 0301-0449
Elektronische ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-015-3518-2

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