Floppy infant caused by MTM1 mutation: a first genetically-confirmed X-linked myotubular myopathy patient in Thailand.

Abstract

Floppy infant syndrome (FIS) refers to a condition wherein an infant manifests generalized hypotonia since birth or in early life. It is heterogeneous and can be caused by various central nervous system disorders, neuromuscular diseases and genetic disorders. X-linked myotubular myopathy (XMTM) is a progressive congenital myopathy morphologically characterized by the presence of centrally placed nuclei in numerous muscle fibers without any other particular pathological abnormalities. Patients are frequently born with floppiness and respiratory distress. The vast majority of patients carry a truncating or missense mutation in MTM1. The authors report here a full term male baby with clinicopathological features of XMTM. The diagnosis is validated by the finding of a c. 141-144delAGAA mutation ofMTM1. To the best of the authors' knowledge, the present case is the first genetically confirmed XMTM in Thailand. A brief review of various neuromuscular disorders causing floppy infant syndrome is also included.

• Authors: Teerin Liewluck, Natte Raksadawan, Chanin Limwongse, Ichizo Nishino, Tumtip Sangruchi
• Journal: Journal of the Medical Association of Thailand = Chotmaihet thangphaet (J Med Assoc Thai) Vol. 89 Issue 1 Pg. 99-105 (Jan 2006) ISSN: 0125-2208 [Print] Thailand
• PMID: 16583589 (Publication Type: Case Reports, Journal Article)

Chemical References

• Protein Tyrosine Phosphatases
• Protein Tyrosine Phosphatases, Non-Receptor
• myotubularin

Topics

• Chromosome Mapping
• Chromosomes, Human, X
• DNA Mutational Analysis
• Genetic Diseases, X-Linked (diagnosis, ethnology, genetics)
• Humans
• Infant, Newborn
• Male
• Myopathies, Structural, Congenital (diagnosis, genetics, pathology)
• Pedigree
• Protein Tyrosine Phosphatases (genetics)
• Protein Tyrosine Phosphatases, Non-Receptor
• Thailand