Two sisters with prenatal growth failure, disproportionate short stature, and feeding difficulties
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Updated: Oct 27, 2026

A Common Marmoset Model of Mother-Infant Intervention for Breastfeeding Disorders in the Presence of Paternal Inhibition and Maternal Neglect
Published on: September 22, 2023
F M Cameron1, A D Cameron, L Crampin
1Department of Child Health, Royal Hospital for Sick Children, Glasgow, UK.
Abstract:
A familial short stature syndrome is described in two sisters. Clinical features include severe pre- and post-natal growth failure, stridor, feeding difficulties in the first 2 years requiring nasogastric feeding and facial dysmorphism reminiscent of Three M syndrome. Intellectual function is normal. Skeletal surveys show short long bones, small square iliac bones, short femoral necks and vertebral bodies which are short in the antero-posterior diameter with narrowing of the interpedicular distance inferiorly.
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