The Journal of Pediatrics
Volume 146, Issue 4 , Pages 537-541, April 2005

Midline defects in FG syndrome: Does tethered spinal cord contribute to the phenotype?

From Medical Genetics Institute, Steven Spielberg Pediatric Research Center, Department of Pediatrics, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, California; the Department of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, Georgia; and Maxine Dunitz Neurosurgical Institute, Department of Pediatric Neurosurgery, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, California

Received 11 June 2004; received in revised form 15 September 2004; accepted 19 October 2004.

Objectives

FG syndrome is an X-linked recessive mental retardation syndrome with ano-rectal anomalies, constipation, and occasional urinary incontinence. Because tethered spinal cord syndrome (TCS) has similar symptoms, we evaluated imaging for TCS in patients with FG syndrome.

Study design

Patients were recruited from the International FG Syndrome Support Group, and an FG Syndrome Consensus Group reviewed clinical histories, medical records, and photographs of each responding patient. Results of cranial and spinal imaging studies were available for 12 patients.

Results

Of 12 boys with FG syndrome, 6 had hypoplasia of the corpus callosum, and 3 of these had TCS (all with constipation and urinary symptoms). The other 9 did not have urinary symptoms. After surgical untethering, bowel and bladder symptoms improved.

Conclusions

Tethered spinal cord syndrome occurred in 25% of patients with FG syndrome associated with hypoplasia of the corpus callosum and causing bowel and bladder incontinence. A high index of suspicion is necessary for early diagnosis, and timely intervention results in significant improvement in symptomatology.

ACC, Agenesis of the corpus callosum, TCS, Tethered spinal cord syndrome

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 30.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Supported by SHARE's Child Disability Center, UCLA Intercampus NIH/NIGMS Medical Genetics Training Program grant GM08243 and NIH/NICHD grant HD22657 from the US Department of Health and Human Services (J.M.G.) and NIH Clinical Research LRP MD000625-01 (J.V.).

PII: S0022-3476(04)01009-1

doi:10.1016/j.jpeds.2004.10.050

The Journal of Pediatrics
Volume 146, Issue 4 , Pages 537-541, April 2005