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Little Ella s weight loss baffled doctors for months - now her family want to raise awareness of a condition no one has ever heard of
Ella Cooper was diagnosed with Wiedemann–Steiner syndrome at 22-months-old
Ella Cooper (Image: Kay Garratt)
The parents of a little girl who wasn t putting on weight due to a rare genetic syndrome now want to raise awareness after her diagnosis.
Ella Cooper stopped breathing after she was born at Tameside Hospital on New Year s Day 2019.
Her mum Kay Garratt, 38, said she was then never very well as a baby, with doctors first believing that she had a dairy allergy.