Radiological characteristics of skeletal growth in neonates and infants with achondroplasia

Author:

Miyahara Daisuke12,Hasegawa Kosei3ORCID,Ago Yuko3,Futagawa Natsuko13,Miyahara Hiroyuki1,Higuchi Yousuke3,Yamada Kazuki4,Tetsunaga Tomonori4,Moriwake Tadashi5,Tanaka Hiroyuki6,Tsukahara Hirokazu1

Affiliation:

1. Department of Pediatrics, Okayama University Graduate School of Medicine Dentistry and Pharmaceutical Sciences Okayama Japan

2. Department of Pediatrics Hiroshima City Hiroshima Citizens Hospital Hiroshima Japan

3. Department of Pediatrics Okayama University Hospital Okayama Japan

4. Department of Orthopedics Okayama University Hospital Okayama Japan

5. Department of Pediatrics, Iwakuni Clinical Center National Hospital Organization Iwakuni Japan

6. Department of Pediatrics Okayama Saiseikai General Hospital Okayama Japan

Abstract

AbstractAchondroplasia (ACH) is the most common form of skeletal dysplasia characterized by a rhizomelic short stature. Radiological skeletal findings in pediatric and adult patients with ACH include short long bones, a relatively longer fibula compared to the tibia, a narrow lumbar interpedicular distance, and a hypoplastic iliac wing. Nonetheless, the characteristics of skeletal growth during the neonatal and infantile periods have scarcely been explored. Therefore, this retrospective study aimed to analyze the radiological skeletal growth during the neonatal and infantile periods in 41 Japanese patients with genetically confirmed ACH. The length of long bones in the upper and lower limbs and the lumbar interpedicular distances at L1 and L4 were measured. These parameters showed significant positive correlations with age. The upper segment‐to‐lower segment ratio in the lower limbs resembled the data of healthy controls from previous reports. The L1/L4 and fibula/tibia ratios increased with age, suggesting that some representative skeletal phenotypes of ACH were less distinct during the neonatal and infantile periods. In conclusion, for the first time, this study radiologically characterized skeletal growth during the neonatal and infantile periods of patients with genetically confirmed ACH.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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