Familial infantile myasthenia (Q92758): Difference between revisions
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15 August 2026
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Latest revision as of 07:53, 16 August 2026
Isolated Prolyl endopeptidase-like (PREPL) deficiency causing congenital myasthenic syndromes with pre- and postsynaptic features and growth hormone deficiency was reported in a singleton case. Clinical features include onset at birth, hypotonia, feeding difficulties. On examination eyelid ptosis, tented upper lip, proximal muscle weakness, variable during day, cholinesterase-inhibitor responsive. No decrement on repetitive nerve stimulation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1087841084 |
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| English | Familial infantile myasthenia |
Isolated Prolyl endopeptidase-like (PREPL) deficiency causing congenital myasthenic syndromes with pre- and postsynaptic features and growth hormone deficiency was reported in a singleton case. Clinical features include onset at birth, hypotonia, feeding difficulties. On examination eyelid ptosis, tented upper lip, proximal muscle weakness, variable during day, cholinesterase-inhibitor responsive. No decrement on repetitive nerve stimulation. |
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CID11:ID_1087841084
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dki-india-ID_1087841084
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Concluído
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15 August 2026
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