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Down Syndrome, Achondroplasia and Tetralogy of Fallot
by
McCrossan, Brian A.
, Sweeney, Louise
, Dabir, Tabib
, Magee, Alex
, Sands, Andrew J.
in
Achondroplasia - complications
/ Achondroplasia - diagnosis
/ Achondroplasia - genetics
/ Case Report
/ Down Syndrome - complications
/ Down Syndrome - diagnosis
/ Down Syndrome - genetics
/ Fatal Outcome
/ Female
/ Humans
/ Infant
/ Karyotyping
/ Mutation - genetics
/ Receptors, Fibroblast Growth Factor - genetics
/ Respiratory Insufficiency - etiology
/ Tetralogy of Fallot - complications
/ Tetralogy of Fallot - diagnosis
/ Tetralogy of Fallot - genetics
2008
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Down Syndrome, Achondroplasia and Tetralogy of Fallot
by
McCrossan, Brian A.
, Sweeney, Louise
, Dabir, Tabib
, Magee, Alex
, Sands, Andrew J.
in
Achondroplasia - complications
/ Achondroplasia - diagnosis
/ Achondroplasia - genetics
/ Case Report
/ Down Syndrome - complications
/ Down Syndrome - diagnosis
/ Down Syndrome - genetics
/ Fatal Outcome
/ Female
/ Humans
/ Infant
/ Karyotyping
/ Mutation - genetics
/ Receptors, Fibroblast Growth Factor - genetics
/ Respiratory Insufficiency - etiology
/ Tetralogy of Fallot - complications
/ Tetralogy of Fallot - diagnosis
/ Tetralogy of Fallot - genetics
2008
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Down Syndrome, Achondroplasia and Tetralogy of Fallot
by
McCrossan, Brian A.
, Sweeney, Louise
, Dabir, Tabib
, Magee, Alex
, Sands, Andrew J.
in
Achondroplasia - complications
/ Achondroplasia - diagnosis
/ Achondroplasia - genetics
/ Case Report
/ Down Syndrome - complications
/ Down Syndrome - diagnosis
/ Down Syndrome - genetics
/ Fatal Outcome
/ Female
/ Humans
/ Infant
/ Karyotyping
/ Mutation - genetics
/ Receptors, Fibroblast Growth Factor - genetics
/ Respiratory Insufficiency - etiology
/ Tetralogy of Fallot - complications
/ Tetralogy of Fallot - diagnosis
/ Tetralogy of Fallot - genetics
2008
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Journal Article
Down Syndrome, Achondroplasia and Tetralogy of Fallot
2008
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Overview
This paper describes a female infant with achondroplasia, Down syndrome and tetralogy of Fallot. Down syndrome and achondroplasia were confirmed by karyotyping and presence of a common fibroblast growth factor receptor 3 mutation (Gly380Arg), respectively. The clinical course was complicated by pulmonary hypoplasia and subsequent intractable respiratory failure secondary to the combination of congenital conditions, which resulted in the patient’s death at 5 months.
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