A boy was referred in 1977 for investigation of global retardation and hypotonia. Minor dysmorphic features and intractable constipation were noted. In 1981 the mother's sister had a son with a similar phenotype. This is probably the X linked Opitz-Kaveggia or FG syndrome.
No takes yet. Share an insight, caveat, or question.
Burn et al. (1983) studied this question.
Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context: