RECENTLY RECOGNIZED CONGENITAL MYASTHENIC SYNDROMES: (A) END‐PLATE ACETYLCHOLINE (ACH) ESTERASE DEFICIENCY (B) PUTATIVE ABNORMALITY OF THE ACH INDUCED ION CHANNEL (C) PUTATIVE DEFECT OF ACH RESYNTHESIS OR MOBILIZATION‐CLINICAL FEATURES, ULTRASTRUCTURE AND CYTOCHEMISTRY*