|Year : 2004 | Volume
| Issue : 2 | Page : 254--256
Congenital fiber type disproportion: A rare type of congenital myopathy: A report of four cases
MC Sharma1, AM Ralte1, SK Atri1, S Gulati2, V Kalra2, Chitra Sarkar1,
1 Departments of Pathology, All India Institute of Medical Sciences, New Delhi, India
2 Departments of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Professor of Pathology, Department of Pathology, All India Institute of Medical Sciences, New Delhi - 110029
Congenital fiber type disproportion is a rare type of congenital myopathy which presents as hypotonia, delayed motor milestones and dysmorphic facies. During the past 2 years we received 449 muscle biopsies, of which 4 cases were diagnosed as congenital fiber type disproportion (CFTD). In addition to CFTD, one case also had centronuclear features. Three of them were females and one was a male child. Although rare, it should be considered in the differential diagnosis of childhood muscle diseases. Histochemical staining is necessary for the diagnosis of this entity.
|How to cite this article:|
Sharma M C, Ralte A M, Atri S K, Gulati S, Kalra V, Sarkar C. Congenital fiber type disproportion: A rare type of congenital myopathy: A report of four cases.Neurol India 2004;52:254-256
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Sharma M C, Ralte A M, Atri S K, Gulati S, Kalra V, Sarkar C. Congenital fiber type disproportion: A rare type of congenital myopathy: A report of four cases. Neurol India [serial online] 2004 [cited 2021 Sep 17 ];52:254-256
Available from: https://www.neurologyindia.com/text.asp?2004/52/2/254/11058
Congenital fiber type disproportion (CFTD) is a rare type of congenital myopathy which was first described by Brooke in 1973 and since then about 36 cases have been described in the literature. This disease is transmitted as an autosomal recessive trait but exceptions have been reported., CFTD is clinically characterized by hypotonia and delayed motor milestones, and histologically, Type I fibers are smaller than Type II fibers and there is a predominance of the former.
We describe four rare cases of CFTD which we encountered in the past two years.
A 17-year-old female presented with history of progressive muscle weakness of both lower limbs which started at the age of 10 years. There was history of delayed motor milestones. Examination revealed normal facies, and muscle bulk, tone and power was normal. Electrophysiological studies (EPS) revealed myopathic pattern and normal creatine phosphokinase (CPK) level. Muscle biopsy was done with a clinical diagnosis of limb girdle muscular dystrophy.
A three and half-year-old-male child presented with history of inability to walk and feeding difficulties. He was the first child of a non-consanguineous marriage. Examination revealed long facies, eyelid drooping (ptosis), high arched palate and squint. Muscle tone was decreased and reflexes were absent. Genetic studies revealed no SMA gene deletions. CPK level was normal (CPK-59 IU/L). Muscle biopsy was done with a clinical diagnosis of congenital myopathy.
A 4-year-old female child presented with history of frequent falls and ptosis of 3 years duration. Antenatal history was uneventful and she was a product of a non-consanguineous marriage. Examination showed high arched palate, flat foot, ptosis and squint. Muscle tone was normal and EMG showed myopathic changes. CPK level was 182 IU/L. Muscle biopsy was done with a clinical diagnosis of congenital myopathy.
A 12-year-old female child presented with history of decreased movements since birth and delayed motor milestones. Examination revealed large head, low set ears, and facial dysmorphism. There was generalized hypotonia and reflexes were sluggish. EPS revealed myopathic changes and CPK was raised (455 IU/L).
Muscle biopsy in all cases shows similar features with minor variations. The majority of the fibers were small in diameter [Figure:1]a but no angulated fibers were seen. A small percentage of fibers were either of normal diameter or appeared to be hypertrophied. There was no myophagocytosis and regeneration and degenerating fibers were not seen. Endomysial and perimysial fibrosis was minimal or absent.
In all cases except Case 2, there was predominance of Type I fibers. This feature was better appreciated on NADH-TR [Figure:1]b and ATPase stains. In Case 2 there was predominance of Type II fibers [Figure:1]c. All the small fibers were of similar type. In addition to fiber type disproportion, Case 4 also revealed central nuclei in the majority of the fibers and oxidative stains revealed a perinuclear halo in this case [Figure:1].
Congenital fibre type disproportion (CFTD) is characterized by congenital hypotonia and delayed motor milestones, often associated with congenital dislocation of the hip joint, high arched palate, kyphoscoliosis and contractures. EMG shows myopathic pattern and the CPK level is normal or mildly elevated. Rarely, associated cardiomyopathies have been reported. Histologically, the muscle biopsy shows relatively smaller fibers (at least 25%) of Type I as compared to Type II fibers. Type II fibers are either of normal size or hypertrophied and there is a predominance of Type I fibres., All the cases under discussion, except Case 2 revealed hypoplasia and predominance of Type I fibers.
In addition, Case 4 showed central nuclei in a significant number of fibers. This has been reported earlier either at the time of first diagnosis or in a repeat biopsy after an interval of 41 months. Even a change from CFTD to myopathic features like LGMD has been described in the sequential biopsies.
Interestingly, our Case 2 showed hypoplasia and predominance of Type II fibers and hypertrophy of Type 1 fibers.
Morphologically, a close differential diagnosis of this condition is neurogenic atrophy like spinal muscular atrophy (SMA). In the absence of atrophied and angulated fibers, hypoplasia of only Type I fibers and lack of type grouping the possibility of the latter is excluded.
We conclude that CFTD is a rare type of congenital myopathy and should be considered in the differential diagnoses of early onset myopathies. Histochemical staining is necessary for its diagnosis and differentiation from other myopathies and spinal muscular atrophy.
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