Apert syndrome

Apert syndrome
Dr Trisha Macnair
Some genetic conditions lie hidden away deep within the cells, causing mischief that may not be very apparent, at least until later in life.
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Apert Syndrome
Aphthous Ulcer (Canker Sores)
Apolipoprotein B Deficiency (Bassen-Kornzweig Syndrome)
Apoplexy
Appendicitis ...
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The best-known type of acrocephalosyndactyly is Apert syndrome which is due to a mutation in the fibroblast growth factor receptor 2 (FGFR2) gene on chromosome 10.
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Normal ridging due to overlap of bony plates after birth -- resolves spontaneously
Congenital craniosynostosis
Crouzon's syndrome
Apert syndrome
Carpenter's syndrome
Pfeiffer syndrome ...
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if the baby has Apert syndrome, a congenital condition that causes multiple abnormalities
if the baby has Crouzon's disease, a congenital disease that causes abnormalities of the face, as well as other disorders ...
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