Literature DB >> 12922003

[Unusual good prognosis for X-linked myotubular myopathy].

S Chanzy1, M C Routon, S Moretti, C de Gennes, J C Mselati.   

Abstract

Recessive X-linked myotubular myopathy has recently been shown to be linked to the mutation of a gene located in the Xq28 region. Evolution is used to be considered as fatal but mild forms or forms with a better prognosis have been recorded since. We report a case in a patient, whose parents were warned of fatal outcome once the diagnosis was made during the neonatal period. The reaction of the parents was to avoid any relationship with medical care. Ten years later the patient was seen in relatively good health thus proving that the evolution was more favourable than anticipated.

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Year:  2003        PMID: 12922003     DOI: 10.1016/s0929-693x(03)00287-2

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  3 in total

1.  X-linked myotubular myopathy in a family with two infant siblings: a case with MTM1 mutation.

Authors:  Ji Hyun Jeon; Ran Namgung; Min Soo Park; Kook In Park; Chul Lee; Jin Sung Lee; Se Hoon Kim
Journal:  Yonsei Med J       Date:  2011-05       Impact factor: 2.759

2.  Muscle pathology, limb strength, walking gait, respiratory function and neurological impairment establish disease progression in the p.N155K canine model of X-linked myotubular myopathy.

Authors:  Melissa A Goddard; David L Mack; Stefan M Czerniecki; Valerie E Kelly; Jessica M Snyder; Robert W Grange; Michael W Lawlor; Barbara K Smith; Alan H Beggs; Martin K Childers
Journal:  Ann Transl Med       Date:  2015-10

Review 3.  Centronuclear (myotubular) myopathy.

Authors:  Heinz Jungbluth; Carina Wallgren-Pettersson; Jocelyn Laporte
Journal:  Orphanet J Rare Dis       Date:  2008-09-25       Impact factor: 4.123

  3 in total

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