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 towerskull) anomalies were considered to be relatively minor. The adverse drug reaction ... Cited by 2 - Related articles - All 5 versions
SA Feig, GB Segel… - Chronic Complex Diseases of …, 2011 - books.google.com ... This, in turn, leads to maxillary hypertrophy, towerskull (“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 (towerskull and prominent maxilla). ... Related articles
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 ... Related articles - All 2 versions
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