A Wide Spectrum of Axial Mesodermal Dysplasia Complex With Rhombencephalic Anomaly: A Case Report

被引:4
|
作者
Kim, Kang-Won [1 ]
Seo, Jeoung-Hwan [1 ]
Ko, Myoung-Hwan [1 ]
Won, Yu-Hui [1 ]
Park, Sung-Hee [1 ]
机构
[1] Chonbuk Natl Univ, Med Sch, Dept Phys Med & Rehabil, 567 Baekje Daero, Jeonju 54896, South Korea
来源
ANNALS OF REHABILITATION MEDICINE-ARM | 2016年 / 40卷 / 01期
关键词
Axial mesodermal dysplasia spectrum; Medulla oblongata; Rhombencephalon;
D O I
10.5535/arm.2016.40.1.162
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Axial mesodermal dysplasia complex (AMDC) arises in variable combinations of craniocaudal anomalies such as musculoskeletal deformities, neuroschisis, or rhombencephalic developmental disorders. To the best of our knowledge, the co-existence of AMDC with associated musculoskeletal anomalies, medullary neuroschisis with mirror movements, and cranial nerve anomalies has not yet been reported. Here, we report the case of a 4-year-old boy whose clinical features were suggestive of Goldenhar syndrome and Poland syndrome with Sprengel deformity. Moreover, he showed mirror movements in his hands suspected of rhombencephalic malformation, and infranuclear-type facial nerve palsy of the left side of his face, the opposite side to the facial anomalies of Goldenhar syndrome. After conducting radiological studies, he was diagnosed with medullary neuroschisis without pontine malformations and Klippel-Feil syndrome with rib anomalies. Based on these findings, we propose that clinical AMDC can be accompanied by a wide variety of musculoskeletal defects and variable degrees of central nervous system malformations. Therefore, in addition to detailed physical and neurological examinations, imaging studies should be considered in AMDC.
引用
收藏
页码:162 / 167
页数:6
相关论文
共 50 条
  • [33] Case Report: Wide Spectrum of Manifestations of Ligase IV Deficiency: Report of 3 Cases
    Costa e Castro, Ana
    Maia, Raquel
    Batalha, Sara
    Freixo, Joao Parente
    Martins, Catarina
    Neves, Conceicao
    Cordeiro, Ana Isabel
    Neves, Joao Farela
    FRONTIERS IN IMMUNOLOGY, 2022, 13
  • [36] HOW WIDE IS THE CLINICAL SPECTRUM OF THE ACROCALLOSAL SYNDROME - REPORT OF A MILD CASE
    TUROLLA, L
    CLEMENTI, M
    TENCONI, R
    JOURNAL OF MEDICAL GENETICS, 1990, 27 (08) : 516 - 518
  • [37] The wide spectrum of cerebrotendinous xanthomatosis: Case report of a rare but treatable disease
    Rosafio, Francesca
    Cavallieri, Francesco
    Guaraldi, Pietro
    Taroni, Franco
    Nichelli, Paolo Frigio
    Mandrioli, Jessica
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2016, 143 : 1 - 3
  • [38] Antiphospholipid syndrome: a case report with an unusual wide spectrum of clinical manifestations
    Mazzoccoli, Carmela
    Comitangelo, Domenico
    D'Introno, Alessia
    Mastropierro, Valeria
    Sabba, Carlo
    Perrone, Antonio
    AUTOIMMUNITY HIGHLIGHTS, 2019, 10 (01)
  • [39] Myoclonic epilepsy, cortical dysplasia and mitochondrial complex I deficiency: A case report
    Nesti, C.
    Mancuso, M.
    Petrozzi, L.
    Santorelli, F. M.
    Rocchi, A.
    Ali, G.
    Tessa, A.
    LoGerfo, A.
    Iudice, A.
    Siciliano, G.
    NEUROMUSCULAR DISORDERS, 2009, 19 (8-9) : 563 - 564
  • [40] At Both Ends of the Spectrum: A Case Report of an Infant with Anauxetic Dysplasia and Severe Combined Immunodeficiency
    Zayia, Lindsay
    Niebur, Hana
    Velasco, Danita
    JOURNAL OF CLINICAL IMMUNOLOGY, 2021, 41 (SUPPL 1) : S123 - S124