Pseudoaminopterin syndrome.

Abstract

Pseudoaminopterin syndrome or aminopterin syndrome-like sine aminopterin (ASSA syndrome--OMIM 600325] is a rare autosomal recessive syndrome defined by characteristic dysmorphic features, skeletal defects, limb anomalies, cryptorchidism, and growth retardation. The syndrome owes its name to the fact that patients resemble the children exposed to aminopterin or to methotrexate, two dihydrofolate reductase inhibitors used for chemotherapy, or as an abortificient in early pregnancy. Ten patients have been described with pseudoaminopterin syndrome. Their phenotype is variable, and differs from the phenotype resulting from folic acid deprivation, leading to the notion that the pathogenesis may be more complex than simple vitamin deficiency. We report on an Algerian patient with pseudoaminopterin syndrome, review the previously reported cases and confirm that pseudoaminopterin syndrome does not result from a detectable contiguous gene imbalance as high resolution CGH array was normal in this child.

• Authors: Lilia Kraoua, Yline Capri, Laurence Perrin, Abdelmajjid Benmansour, Alain Verloes
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) Vol. 158A Issue 9 Pg. 2233-8 (Sep 2012) ISSN: 1552-4833 [Electronic] United States
• PMID: 22811276 (Publication Type: Case Reports, Journal Article)
• Copyright: Copyright © 2012 Wiley Periodicals, Inc.

Topics

• Abnormalities, Multiple (diagnosis, genetics, physiopathology)
• Adult
• Craniofacial Abnormalities (diagnosis, genetics, physiopathology)
• Female
• Humans
• Infant, Newborn
• Intellectual Disability (diagnosis, genetics, physiopathology)
• Male