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VJ Karthikeyan, RE Ferner, S Baghdadi… - Journal of …, 2011 - journals.lww.com
... Results: Eight (8.8%) of the pregnancies led to an infant with a developmental
anomaly, but all save one of these (craniosynostosis with tower skull) anomalies
were considered to be relatively minor. The adverse drug reaction ...
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SA Feig, GB Segel… - Chronic Complex Diseases of …, 2011 - books.google.com
... This, in turn, leads to maxillary hypertrophy, tower skull (“thalassemic facies”),
hepatosplenomegaly, and increased risk of bone fractures. Long term sequelae include higher
risk of cholelithiasis and cholecystitis as well as pulmonary hyper- tension. ...
Related articles
SA Feig, GB Segel… - Chronic Complex Diseases of …, 2011 - books.google.com
... Severely affected patients may develop marrow hypertrophy with prominent maxilla, tower
skull, thinning of cortical bone and splenomegaly. These children are at risk of splenic rupture
and fractures of thin cortical bone after relatively minor trauma. ...
Related articles
SA Feig, GB Segel… - Chronic Complex Diseases of …, 2011 - books.google.com
... Severe β-thalassemia major causes severe hypochromic, microcytic anemia, hepatosplenomegaly,
and jaundice. Expansion of the marrow space causes thinning of the bones, susceptibility to
fractures, and typical thalassemic facies (tower skull and prominent maxilla). ...
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M Zoli, D Mazzatenta, E Pasquini, P Ambrosetto… - Pituitary, 2011 - Springer
... beyond the confines of sella turcica. Br J Surg 39:7–24 7. Uhthoff W (1914) Ophtalmic
experiences and considerations on the surgery of cerebral tumours and the tower
skull the Bowman Lecture. Tr Ophth Soc UK 34:xvii–cxxiii ...
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