Radiological evolution in IMAGe association: A case report

被引:12
作者
Amano, Naoko
Naoaki, Hori
Ishii, Tomohiro
Narumi, Satoshi
Hachiya, Rumi
Nishimura, Gen [2 ]
Hasegawa, Tomonobu [1 ]
机构
[1] Keio Univ, Sch Med, Dept Pediat, Shinjuku Ku, Tokyo 1608582, Japan
[2] Tokyo Metropolitan Kiyose Childrens Hosp, Dept Radiol, Tokyo, Japan
关键词
IMAGe association; metaphyseal dysplasia; adrenal hypoplasia congenita;
D O I
10.1002/ajmg.a.32425
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
IMAGe association is a recently recognized multi-system disorder of unknown etiology. IMAGe is a mnemonic acronym that stands for Intrauterine growth retardation, Metaphyseal dysplasia, Adrenal hypoplasia congenita, and Genital anomalies (OMIM 300290). Suspicion for the disorder is readily raised by the distinctive clinical and endocrinological constellation, and radiological identification of metaphyseal dysplasia is crucial for the diagnosis. However, knowledge of the onset, evolution, severity, and variation of the metaphyseal dysplasia is currently limited. We illustrate the radiological evolution of an affected girl from her premature birth to early childhood. Her initial skeletal changes included thin ribs, delayed ossification of the juxtatruncal bones, and delayed epiphyseal ossification. The former two became less conspicuous during infancy. Metaphyseal dysplasia was not discerned at birth. However, mild metaphyseal cupping, sclerosis and longitudinal striations became manifest in late infancy, and then progressed with age. It is thought that the skeletal alterations in IMAGe association encompass retarded endochondral ossification normalized later on and mild metaphyseal dysplasia of postnatal onset. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:2130 / 2133
页数:4
相关论文
共 11 条
[1]   A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans [J].
Achermann, JC ;
Ito, M ;
Ito, M ;
Hindmarsh, PC ;
Jameson, JL .
NATURE GENETICS, 1999, 22 (02) :125-126
[2]   Gonadal determination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner [J].
Achermann, JC ;
Ozisik, G ;
Ito, M ;
Orun, UA ;
Harmanci, K ;
Gurakan, B ;
Jameson, JL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (04) :1829-1833
[3]   Familial occurrence of the IMAGe association:: Additional clinical variants and a proposed mode of inheritance [J].
Bergadá, I ;
del Rey, G ;
Lapunzina, P ;
Bergadá, C ;
Fellous, M ;
Copelli, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (06) :3186-3190
[4]  
Blethen SL, 1990, DYSMORPH CLIN GENET, V4, P110
[5]  
Ferey S, 2003, J RADIOL, V84, P323
[6]   IMAGe association: Additional clinical features and evidence for recessive autosomal inheritance [J].
Lienhardt, A ;
Mas, JC ;
Kalifa, G ;
Chaussain, JL ;
Tauber, M .
HORMONE RESEARCH, 2002, 57 :71-78
[7]   MUTATIONS IN THE DAX-1 GENE GIVE RISE TO BOTH X-LINKED ADRENAL HYPOPLASIA CONGENITA AND HYPOGONADOTROPIC HYPOGONADISM [J].
MUSCATELLI, F ;
STROM, TM ;
WALKER, AP ;
ZANARIA, E ;
RECAN, D ;
MEINDL, A ;
BARDONI, B ;
GUIOLI, S ;
ZEHETNER, G ;
RABL, W ;
SCHWARZ, HP ;
KAPLAN, JC ;
CAMERINO, G ;
MEITINGER, T ;
MONACO, AP .
NATURE, 1994, 372 (6507) :672-676
[8]   IMAGe syndrome: A complex disorder affecting growth, adrenal and gonadal function, and skeletal development [J].
Pedreira, CC ;
Savarirayan, R ;
Zacharin, MR .
JOURNAL OF PEDIATRICS, 2004, 144 (02) :274-277
[9]   Two sisters with IMAGe syndrome: Cytomegalic adrenal histopathology, support for autosomal recessive inheritance and literature review [J].
Tan, Tiong Yang ;
Jameson, J. Larry ;
Campbell, Peter Ellis ;
Ekert, Paul G. ;
Zacharin, Margaret ;
Savarirayan, Ravi .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (16) :1778-1784
[10]   Cephaloskeletal dysplasia (Taybi-Linder syndrome; osteodysplastic primordial dwarfism type III): report of two cases and review of the literature [J].
Vichi, GF ;
Currarino, G ;
Wasserman, RL ;
Duvina, PL ;
Filippi, L .
PEDIATRIC RADIOLOGY, 2000, 30 (09) :644-652