Cover image of the article: Pseudoachondroplasia: A Rare Cause of Short Limbed Dwarfism

Image Credit:J Compr Ped

Pseudoachondroplasia: A Rare Cause of Short Limbed Dwarfism

Authors

K Jagadish Kumar1,*, Nayana Nayana1, V G Manjunath1, Chandrashekar Shetty1
1JSS Medical College, Mysore, India
*Corresponding Author: Corresponding author: K Jagadish Kumar, JSS Medical College, Mysore, India. E-mail: Email: jagdishmandya@gmail.com

Journal of Comprehensive Pediatrics:Vol. 8, issue 1; e39867
Published online:Feb 27, 2017
Article type:Case Report
Received:Jun 14, 2016
Accepted:Feb 07, 2017
How to Cite:Kumar KJ, Nayana N, Manjunath VG, Shetty C. Pseudoachondroplasia: A Rare Cause of Short Limbed Dwarfism. J Compr Ped. 2017;8(1):e39867. doi: https://doi.org/10.5812/compreped.39867

Abstract

Pseudoachondroplasia is a rare type of short-limbed skeletal dysplasia. It is usually found as an autosomal dominant inheritable disorder. Children are normal at birth and they present developmental delay in walking by the age of 2, an abnormal waddling gait or deformities of the lower limb. Diagnosis is based on characteristic clinical and radiological findings. This study reports on a 6-year-old boy with classical features of pseudoachondroplasia.

Highlights

1. Introduction

Pseudoachondroplasia (PSACH) is a rare type of short-limbed dwarfism. The prevalence of Pseudoachondroplasia is approximately 4 per 1 million individuals (1). It is usually found as an autosomal dominant disorder, yet somatic or germline mosaicism has also been reported. Children are normal at birth and they usually present short stature, a delay in walking, an abnormal waddling gait or lower limb deformity at 2 to 3 years of age. Radiologically both epiphysis and metaphysis will be affected.

2. Case Presentation

A 6-year-old child born of a consanguineous marriage was referred to our hospital for evaluation of short stature. According to the parents, the boy was normal during the first 2 years of life, after which they noticed a short stature and abnormal waddling gait. On examination, the child had height of 84 cm (< 3rd percentile) and upper to lower segment ratio was 1.64:1 suggesting short limbed dwarfism. The child had wrist widening, short stubby fingers, lumbar lordosis and genu varus deformity. The face appeared normal (Figure 1). Systemic examination and intelligent quotient was normal. None of the family members were dwarfs. Skeletal survey was done in view of the short stature.
A, genu varus; B, lumbar lordosis; C, short stubby fingers; D, normal face.
Figure 1.
A, genu varus; B, lumbar lordosis; C, short stubby fingers; D, normal face.
Radiographic findings included a normal skull, with chest X-ray dipicting spatulate ribs with anterior widening. Wrist X-ray revealed delay in bone age with epiphyseal end of bones showing sclerosis, widening, and irregularities. Epiphysis of radius and carpal were less dense and had pencil line outline for expected age. Pelvis showed short thickened femur and tibia, widening of the metaphysis of both of these bones and poorly formed acetabulam. Lumbosacral spine revealed normal interpedicular distance, platyspondyly, superior and inferior rounding of vertebral bodies (Figure 2). Serum calcium, phosphorous, alkaline phosphatase, blood urea, and creatinine were within normal limits. Ultrasound of the abdomen was normal. Based on clinical and radiological features, a diagnosis of pseudoachondroplasia was made.
A, normal interpedicular distance; B, superior and inferior rounding of vertebral bodies; C, short thickened femur and tibia with widening of the metaphysis; D, poorly formed acetabulam; E, pencil line outline for expected age.
Figure 2.
A, normal interpedicular distance; B, superior and inferior rounding of vertebral bodies; C, short thickened femur and tibia with widening of the metaphysis; D, poorly formed acetabulam; E, pencil line outline for expected age.

3. Discussion

Pseudoachondroplasia is an uncommon type of skeletal dysplasia with short limbs, which occurs secondarily to mutations within genes encoding cartilage oligomeric matrix protein (COMP) on chromosome 19. This COMP is present in the extracellular matrix of the ligaments, tendons, and cartilages (1). The disorder was first described by Maroteaux and Lamy in 1959. It is referred as “Achondroplasia with a normal face” (2).
In most families, it runs an autosomal dominant inheritance pattern, however, in some cases, germline or somatic mutations have been reported (3). In our case, the parents and younger siblings were normal, thus indicating the probability of germline or somatic mosaicism in one of the parents. Children are usually invariably normal at birth, and they show a developmental delay in walking, an abnormal waddling gait or deformities of the lower limbs by 2 years of age (4). The case presented here was also normal upto 2 years of age, then presented a waddling gait. In pseudoachondroplasia, length is normal at birth (4). On physical examination, they have normal faces and normal intelligent quotient (5). The adult height usually achieves between 82 and 130 cm with gross shortening of the limbs. Other associated deformities include genu valgum, genu varum, genu recurvatum, elbow extension limitation, kyphoscoliosis, lumbar lordosis, and joint laxity with secondary osteoarthritic changes (1).
The case of the current report also had lumbar lordosis (Figure 1). Lumbar lordosis is observed in around 50% of affected individuals (4). Shortening of the long bones, predominantly of femur and humerus with flared irregular metaphysis are important characteristic findings (5). The radiographic features include, a normal skull, spatulate ribs with anterior widening, pelvis with poorly formed acetabulam with rounded iliac wings. Spine X-ray shows platyspondyly, anterior tongue like projection, superior and inferior rounding of vertebral bodies and normal interpedicular distance. Limb X-ray reveals short thickened femur and tibia with metaphyseal widening.
Ossification of epiphysis is delayed, and when they ossify they are irregular, small, and fragmented. The commonly affected epiphysis are the femoral capital and humeral epiphysis. In the femur bone, medial beaking of the femoral neck is a characteristic finding (5, 6). Hand and foot bones are short, broad with small and rudimentary epiphysis (2). The skull and facial bones are normal (5). The diagnosis of pseudoachondroplasia is based on clinical presentation, examintionl, and radiological findings (4).
The differential diagnoses of pseudoachondroplasia are achondroplasia, multiple epiphyseal dysplasia (MED), and congenital spondyloepiphyseal dysplasia (SED) (4).
Achondroplasia children have a large head with prominent frontal bones and a narrow base. In the lumbar region, the interpedicular distance decreases caudally, yet, with normal vertebral height. Only metaphysis is effected (4). In MED, epiphyses are abnormal with a normal metaphysis, pelvis, and spine. Even though waddling gait is present, yet, is less consistent when compared to pseudoachondroplasia. The spine is usually normal (4, 5). In Spondyloepiphyseal Dysplasia, congenital epiphyseal changes mimic pseudoachondroplasia, yet, spinal changes are more pronounced with marked kyphoscoliosis. Hip joints are affected disproportionately when compared to nearly normal distal limbs (5-7).
Skeletal complications are common in children with Pseudoachondroplasia because of early degeneration of the joints. Therefore, clinicians should diagnose the condition for the purpose of genetic counseling, and early theatment of joint manifestations (5). Many patients have early osteoarthritic changes and joint deformities, which requires orthopedic intervention. At the genetic level, COMP altering therapy can be used to treat this condition (5).

3.1. Conclusion

Pseudoachondroplasia is an uncommon form of short limbed skeletal dysplasia wherein the patients usually have skeletal complications because of early degeneration of the joints.
Early recognition and diagnosis is necessary for genetic counseling and early treatment of joint manifestations.

References

  • 1.
    Herring JA, Tachdjian MO. Pediatric orthopedics. 2. 4th ed. Philadelphia: Saunders; 2008. p. 1702-7.
  • 2.
    Lachman RS. Skeletal dysplasias. The Johns Hopkins University. 2008:2613-70. https://doi.org/10.1016/b978-0-323-04520-9.50173-8.
  • 3.
    Khungar A, Mahajan P, Gupte G, Vasundhara M, Kher A, Bharucha BA. Pseudoachondroplastic dysplasia. J Postgrad Med. 1993;39(2):91-3. [PubMed ID: 8169872].
  • 4.
    Briggs MD, Wright MJ. Pseudoachondroplasia. University of Washington, Seattle; 2004, [updated 2015].
  • 5.
    Tandon A, Bhargava SK, Goel S, Bhatt S. Pseudoachondroplasia: A rare cause of rhizomelic dwarfism. Indian J Orthop. 2008;42(4):477-9. [PubMed ID: 19753240]. https://doi.org/10.4103/0019-5413.43400.
  • 6.
    Radlovic V, Smoljanic Z, Radlovic N, Jakovljevic M, Lekovic Z, Ducic S, et al. Pseudoachondroplasia: A case report. Srp Arh Celok Lek. 2013;141(9-10):676-9. https://doi.org/10.2298/sarh1310676r.
  • 7.
    Douglas PB, Robert LE, Justin QL, Thomas P. Pseudoachondroplasia. Appl Radiol Online. 2006;35(7).

Copyright

Copyright © 2017, Iranian Society of Pediatrics. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

Similar Articles

25
Aug
2012
Hypercalciuria and Nephrocalcinosis as Early Feature of Wilson Disease Onset: Description of a Pediatric Case and Literature Review

Hypercalciuria and Nephrocalcinosis as Early Feature of Wilson Disease Onset: Description of a Pediatric Case and Literature Review

Valeria Di Stefano,
Elena Lionetti,
Novella Rotolo,
Mario La Rosa,
Salvatore Leonardi

Di Stefano V, Lionetti E, Rotolo N, La Rosa M, Leonardi S. Hypercalciuria and Nephrocalcinosis as Early Feature of Wilson Disease Onset: Description of a Pediatric Case and Literature Review. Hepat Mon. 2012;12(8):6233. doi: https://doi.org/10.5812/hepatmon.6233

19
Apr
2021
Subcutaneous Calcification and Fixed Flexion Deformity of the Right Elbow Joint in a Child with a GNAS Mutation: A Case Report

Subcutaneous Calcification and Fixed Flexion Deformity of the Right Elbow Joint in a Child with a GNAS Mutation: A Case Report

Hussain Alsaffar,
Najya Attia,
Senthil Senniappan

Alsaffar H, Attia N, Senniappan S. Subcutaneous Calcification and Fixed Flexion Deformity of the Right Elbow Joint in a Child with a GNAS Mutation: A Case Report. Int J Endocrinol Metab. 2021;19(2):e110792. doi: https://doi.org/10.5812/ijem.110792

30
Dec
2006
Atypical Spondylo-Epiphyseal Dysplasia in an Adult Male Patient

Atypical Spondylo-Epiphyseal Dysplasia in an Adult Male Patient  

Gholam Hossein Alishiri

Alishiri GH. Atypical Spondylo-Epiphyseal Dysplasia in an Adult Male Patient  . I J Radiol. 2006;4(1):e79241. doi:

30
Jun
2012
Triple X Syndrome with Short Stature: Case Report and Literature Review

Triple X Syndrome with Short Stature: Case Report and Literature Review

Chaochun Zou,
Mingyan Li,
Zhengyan Zhao

Zou C, Li M, Zhao Z. Triple X Syndrome with Short Stature: Case Report and Literature Review. Inn J Pediatr. 2015;22(2):. doi:

12
Aug
2022
A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report

A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report

Aye Miremarati,
Manijeh Tabrizi,
Setila Dalili,
Seyyedeh Azade Hoseini Nouri

Miremarati A, Tabrizi M, Dalili S, Hoseini Nouri SA. A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report. J Compr Ped. 2022;13(3):e129461. doi: https://doi.org/10.5812/compreped-129461

More by these authors

K Jagadish KumarPubMedScholar
Nayana NayanaPubMedScholar
V G ManjunathPubMedScholar
Chandrashekar ShettyPubMedScholar
Share
Cited by
Metrics