TY - JOUR
TI - Okamoto syndrome in a girl of Caucasian origin
AU - Markouri, M.
AU - Karpathios, T.
AU - Dinopoulos, A.
AU - Attilakos, A.
AU - Fretzayas, A.
AU - Bakoula, C.
AU - Kitsiou-Tzeli, S.
JO - Developmental Medicine and Child Neurology
PY - 2008
VL - 50
TODO - 12
SP - 950-952
PB - 
SN - null
TODO - 10.1111/j.1469-8749.2008.03147.x
TODO - antibiotic agent;  indometacin;  non receptor protein tyrosine phosphatase 2;  protein tyrosine phosphatase;  unclassified drug, article;  barium enema;  case report;  Caucasian;  child;  chromosome 22q;  chromosome duplication;  cleft palate;  clinical feature;  congenital heart disease;  congenital malformation;  constipation;  cystourethrography;  echography;  female;  human;  hydronephrosis;  midface hypoplasia;  muscle hypotonia;  nuclear magnetic resonance spectroscopy;  Okamoto syndrome;  patent ductus arteriosus;  priority journal;  pyeloplasty;  respiratory distress syndrome;  ureteropelvic junction obstruction;  urinary tract infection;  vesicoureteral reflux, Abnormalities, Multiple;  Child, Preschool;  Cleft Palate;  Craniofacial Abnormalities;  Diagnosis, Differential;  DNA Mutational Analysis;  Ductus Arteriosus, Patent;  European Continental Ancestry Group;  Facies;  Female;  Follow-Up Studies;  Humans;  Hydronephrosis;  Infant;  Kidney;  Mental Retardation;  Muscle Hypotonia;  Phenotype;  Syndrome
TODO - We report the clinical and genetic evaluation of a 2-year-old Greek female with striking phenotypic similarities to the three previously published cases of Okamoto syndrome. The main features were characteristic facies, cleft palate, generalized hypotonia, severe developmental delay, congenital hydronephrosis, and congenital heart defects. Routine chromosome testing and whole-genome high-resolution comparative genetic hybridization analysis were negative for any gross numerical or structural chromosome aberrations and for microdeletions/ duplications of more than 3 million base pairs respectively. Fluorescence in situ hybridization analysis for 22q11.2 deletion and DNA analysis of the protein tyrosine phosphatase, non-receptor type II gene were normal, thus excluding DiGeorge and Noonan syndromes. Our patient did not show most of the cardinal features of Schinzel-Giedion, otopalatodigital, and C-trigonocephaly syndromes. Moreover, in our patient some new malformations were identified: unilateral kidney hypoplasia and severe anal stenosis. The latter was considered as pertinent and is described here to establish a wider clinical spectrum of Okamoto syndrome. At the age of 3 years 6 months the child continues to show severe growth failure and significant global developmental delay. For the practising paediatrician it is prudent to bear Okamoto syndrome in mind, especially in children with learning disability and a pattern of dysmorphic features. © 2008 Mac Keith Press.
ER -