Arthrogryposis is a descriptive term, not a specific disease entity: escobar syndrome is an Example.


Journal

Minerva pediatrica
ISSN: 1827-1715
Titre abrégé: Minerva Pediatr
Pays: Italy
ID NLM: 0400740

Informations de publication

Date de publication:
12 Jun 2020
Historique:
entrez: 16 6 2020
pubmed: 17 6 2020
medline: 17 6 2020
Statut: aheadofprint

Résumé

Children born with multiple congenital contractures have been almost always given the diagnosis of arthrogryposis multiplex congenita. Arthrogryposis is a descriptive term, not a specific disease entity. A heterogeneous group of conditions associated with multiple congenital joint contractures (mostly syndromic) should be considered. The records of seven children (four boys and three girls with aged 6months- 11 years) of different ethnic origins have been included in this study. The constellation of specific craniofacial dysmorphic features, spine malformation complex, and appendicular skeletal abnormalities in addition to camptodactyly, talipes equinovarus and rocker- bottom feet were a cluster of malformation complex encountered in our patients. Via comprehensive clinical and imaging study (3D reconstruction CT scan), definite diagnosis of Escobar syndrome has been approached. The clinical and imaging phenotype was the key factor towards etiological understanding, treatment and genotype confirmation. We identified compound heterozygous mutations (c.459dupA [p.Val154Serfs*24] and c.794T>G [p.Leu265Serfs*24] of the CHRNG gene in four patients. Bilateral flexion contractures of the knees have been treated by using Iliazarov external fixator. Simultaneous corrections of scoliosis have been achieved by applying either dual traditional growing rods or single growing rods. The clinical and radiological phenotypic characterizations are the fundamental tool in differentiating Escobar from other forms of multiple contractures. The aim of this study are three folds, firstly to demonstrate the importance of detecting the etiological understanding in children presented with multiple contractures, secondly to refute the general conception among the vast majority of pediatricians and orthopedic surgeons that arthrogryposis multiplex is a diagnostic entity. And thirdly, we were able to detect severe spine deformity via 3D reconstruction CT scan, namely unsegmented posterior spinal bar.

Sections du résumé

BACKGROUND BACKGROUND
Children born with multiple congenital contractures have been almost always given the diagnosis of arthrogryposis multiplex congenita. Arthrogryposis is a descriptive term, not a specific disease entity. A heterogeneous group of conditions associated with multiple congenital joint contractures (mostly syndromic) should be considered.
METHODS METHODS
The records of seven children (four boys and three girls with aged 6months- 11 years) of different ethnic origins have been included in this study. The constellation of specific craniofacial dysmorphic features, spine malformation complex, and appendicular skeletal abnormalities in addition to camptodactyly, talipes equinovarus and rocker- bottom feet were a cluster of malformation complex encountered in our patients. Via comprehensive clinical and imaging study (3D reconstruction CT scan), definite diagnosis of Escobar syndrome has been approached.
RESULTS RESULTS
The clinical and imaging phenotype was the key factor towards etiological understanding, treatment and genotype confirmation. We identified compound heterozygous mutations (c.459dupA [p.Val154Serfs*24] and c.794T>G [p.Leu265Serfs*24] of the CHRNG gene in four patients. Bilateral flexion contractures of the knees have been treated by using Iliazarov external fixator. Simultaneous corrections of scoliosis have been achieved by applying either dual traditional growing rods or single growing rods.
CONCLUSIONS CONCLUSIONS
The clinical and radiological phenotypic characterizations are the fundamental tool in differentiating Escobar from other forms of multiple contractures. The aim of this study are three folds, firstly to demonstrate the importance of detecting the etiological understanding in children presented with multiple contractures, secondly to refute the general conception among the vast majority of pediatricians and orthopedic surgeons that arthrogryposis multiplex is a diagnostic entity. And thirdly, we were able to detect severe spine deformity via 3D reconstruction CT scan, namely unsegmented posterior spinal bar.

Identifiants

pubmed: 32536119
pii: S0026-4946.20.05796-5
doi: 10.23736/S0026-4946.20.05796-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Ali Al Kaissi (A)

First Medical Department, Ludwig Boltzmann Institute of Osteology, Hanusch Hospital of WGKK, AUVA Trauma Centre Meidling, Hanusch Hospital, Vienna, Austria - ali.alkaissi@oss.at.
Paediatric Department, Orthopaedic Hospital of Speising, Vienna, Austria - ali.alkaissi@oss.at.

Sergey Ryabykh (S)

Division Spine Pathology and Rare Diseases, Russian Scientific Ilizarov Center (RISC), Kurgan, Russia.

Polina Ochirova (P)

Division Spine Pathology and Rare Diseases, Russian Scientific Ilizarov Center (RISC), Kurgan, Russia.

Sami Bouchoucha (S)

Pediatric Orthopedic Surgery, Children Hospital, Becher Hamza, Tunis, Tunisia.

Vladimir Kenis (V)

Department of Foot and Ankle Surgery, Neuroorthopaedics and Systemic Disorders, Pediatric Orthopedic Institute n.a. H. Turner, Pushkin, Saint Petersburg, Russia.

Mohammad Shboul (M)

Department of Medical Laboratory Sciences, Jordan University of Science and Technology, Irbid, Jordan.

Rudolf Ganger (R)

Paediatric Department, Orthopaedic Hospital of Speising, Vienna, Austria.

Franz Grill (F)

Paediatric Department, Orthopaedic Hospital of Speising, Vienna, Austria.

Susanne G Kircher (SG)

Department of Medical Chemistry, Medical University of Vienna, Vienna, Austria.

Classifications MeSH