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Prenatal ultrasound and molecular diagnosis elucidate the prognosis of Pfeiffer syndrome
Angie C. Jelin
, Jin Chang
, Vickie Feldstein
, Katherine A. Rauen
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peer-review
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Keyphrases
Pfeiffer Syndrome
100%
Prenatal Ultrasound
100%
Prenatal Genetic Testing
100%
Craniosynostosis
50%
Spine
25%
Molecular Diagnostics
25%
Severe Phenotype
25%
Medical Staff
25%
Broad Thumbs
25%
Midface Hypoplasia
25%
Exon 10
25%
Specific mutation
25%
Cloverleaf Skull
25%
Hypertelorism
25%
Great Toe
25%
Sagittal Craniosynostosis
25%
Ventriculomegaly
25%
FGFR2 Gene
25%
Polyhydramnios
25%
Short Limbs
25%
Ultrasonographic Findings
25%
Orbital Proptosis
25%
Molecular Testing
25%
Medicine and Dentistry
Molecular Diagnosis
100%
Echography
100%
Apert Syndrome
100%
Fetus Echography
100%
Craniofacial Synostosis
75%
Toe
25%
Thumb
25%
Limb
25%
Exophthalmos
25%
Midface Hypoplasia
25%
Exon
25%
Fibroblast Growth Factor Receptor 2
25%
Hypertelorism
25%
Ventriculomegaly
25%
Hydramnios
25%