PEnne Chapters 25-27 OB conditions
The fetal heart is fully formed by
10 weeks
The thickness of the nuchal fold in the second trimester should not exceed
6 mm
Eventration of the diaphragm is best described as
A lack of muscle in the dome of the diaphragm
A protein produced by the yolk sac and fetal liver that is found in excess and the maternal circulation in the presence of a neural tube defect is
AFP
A disorder that results in abnormal bone growth and dwarfism
Achondroplasia
The most common nonlethal skeleton dysplasia is
Achondroplasia
A group of abnormalities associated with the entrapment of fetal parts in fetal amputation is
Amniotic band syndrome
The disorder associated with fetal amputations is
Amniotic band syndrome
Cleft lip and cleft palate may exist with
Amniotic band syndrome, trisomy 13, holoprosencephaly
The following are associated with amniotic band syndrome
Amputation of fetal parts, anencephaly, facial clefting
A cystic hygroma is the result of
An abnormal accumulation of lymphatic fluid within the soft tissue
The absence of the eyes is termed
Anopthalmia
The group of fetal head and brain and normalities that often coexist with spina bifida is referred to as
Arnold Chiari II malformation
There is a normal opening within the _____ septum
Atrial
The form of inheritance in which at least one parent has to be a carrier of an abnormal gene for it to be passed down to the fetus
Autosomal dominant
The following are signs of Arnold Chiari II syndrome
Banana sign, lemon sign, colpocephaly
The following are characteristics of spina bifida cystica, elevated MSAFP
Banana sign, lemon sign, enlarged mass intermedia
The growth disorder syndrome synonymous with organ, skull, and tongue enlargement is
Beckwith Weidman syndrome
Macroglossia is most commonly found with
Beckwith Weidmann syndrome
The measurement obtained between the lateral walls of the orbit is referred to as
Binocular diameter
In VACTERAL association, the C stands for
Cardiac
An absent sacrum and coccyx is referred to as
Caudal regression syndrome
The condition associated with absence of the sacrum and coccyx
Caudal regression syndrome
Close set eyes and nose with a single nostril is termed
Cebocephaly
An abnormal division in the lip is referred to as
Cleft lip
The following are characteristics of spina bifida occulta
Closed defect, sacral dimple, hemangioma
Talipes equinovarus is associated with
Club foot
The narrowing of the aortic arch is indicative of
Coarctation of the aorta
A large, mostly cystic mass is noted in the cervical spine region of the fetus. This most likely represents a
Cystic hygroma
The most common cause of cardiac malposition is
Diaphragmatic hernia
The visualization of the fetal stomach with in the fetal chest is most indicative of
Diaphragmatic hernia
What is also referred to as trisomy 21
Down syndrome
Blood is shunted into the inferior vena cava from the umbilical vein by what structure
Ductus venosus
The condition in which the heart is located outside of the chest wall is termed
Ectopic cordis
A cystic hygroma is found in all of the following conditions
Edwards syndrome, turner syndrome
The fetal lip typically closes by
Eight weeks
And oral teratoma is referred to as
Epignathus
The condition in which there is no nose and a probosics separating two close set orbits
Ethmocephaly
Coexisting pericardial efffusion and pleural effusion is consistent with a diagnosis of
Fetal hydrops
The most common form of diaphragmatic hernia is the
Foramen of Bochdalek
What is the normal opening in the lower middle third of the atrial septum
Foramen ovale
Achondroplasia is associated with the following
Frontal bossing, flat nasal bone, trident hand
Facial anomalies, when discovered, should prompt the sonographer to analyze the brain closely for
Holoprosencephaly
An increase distance between the orbits is referred to as
Hypertelorism
A group of anomalies characterized by a small or absent left ventricle
Hypoplastic left heart syndrome
A group of anomalies characterized by a small or absent right ventricle
Hypoplastic right heart syndrome
The reduction in the distance between the orbits is referred to as
Hypotelorism
Fetal lung maturity can be assessed using the
Lecithin to sphingomyelin ratio
The chamber of the heart closest to the fetal spine is the
Left atrium
In VACTERL association, the letter L stands for
Limb
The thalamic tissue located within the third ventricle of the brain that can become enlarge with Arnold Chiari II malformation
Massa intermedia
Sirenomelia is commonly referred to as
Mermaid syndrome
A small mandible is termed
Micrognathia
The following are characteristics sonographic findings of achondrogenesis
Micromelia absent mineralization of the pelvis, polyhydramnios
The following are sonographic features of pentalogy of Cantrell
Omphalocele, cleft sternum, diaphragmatic hernia
A bell shaped chest and multiple feet or fractures are indicative of
Osteogenesis imperfecta
Upon sonographic interrogation of the 28th week pregnancy, you know that when pressure is applied to the fetal skull, the skull can easily distorted. This is sonographic evidence of
Osteogenesis imperfecta
Sonographic bat wing sign is indicative of
Pleural effusion
The accumulation of fluid around the lungs is termed
Pleural effusion
The following are sonographic features of holoprosencephaly
Probiscis with cyclopia, a fused thalamus, monoventricle
A separate mass of nonfunctioning fetal lung tissue is referred to as
Pulmonary sequestration
Absence of the radius is referred to as
Radial ray defect
The most common fetal cardiac tumor is
Rhabdomyoma
You visualize a mass extending from the distal spine of a fetus. This mass could be all of the following
Sacrococcygeal teratoma, meningocele, meningomyelcele
The abnormal lateral curvature of the spine is referred to as
Scoliosis
Rhizomelia denotes
Shortening of the proximal segment of the limb
What condition is associated with bilateral renal agenesis, oligohydramnios, and fusion of the extremities
Sirenomelia
The following are associated with spina bifida
Splaying of the laminae, Lemon sign, hydrocephalus
What is true concerning fetal outflow tracks
The normal pulmonary artery should be positioned anterior to the aorta and should be visualized crossing over it
Which trisomy is also referred to as Patau syndrome
Trisomy 13
Micrognathia is found in
Trisomy 18
An echogenic intracardiac focus is often seen in cases of
Trisomy 21
Fetal rhabdomyoma a are associated with
Tuberous schlerosis
The embryonic heart begins as
Two tubes
The following are clinical or sonographic findings consistent with limb body wall complex
Ventral wall defect, marked scoliosis, shortened umbilical cord
The following is considered to be the most common cardiac defect
Ventricular septal defect
The following are sonographic signs of Ebstein anomaly
enlarged right atrium, fetal hydrops, malpositioned tricuspid valve
The artifact seen posterior to solid structure such as a fetal bone is referred to as
Acoustic shadowing
The most common cause of hypertelorism is
Anterior cephalocele
Fusion of the orbits is termed
Cyclopia
nuchal thickening is most commonly associated with
Down syndrome
An echogenic intracardiac focus is most often seen in the
Left ventricle
The ventricular septum should be uninterrupted and of equal sickness to that of the _____
Left ventricular wall
An unusual protuberance of the tongue is termed
Macroglossia
Tetralogy of Fallot consists of the following
Overriding aortic root, ventricular septal defect, pulmonary stenosis
The optimal scan plane to visualize micrognathia is
Sagittal
A cloverleaf skull and hydrocephalus is seen with
Thanatophoric dysplasia
The best description of transposition of the great vessels
The aorta arises from the left ventricle and the pulmonary artery arises from the right ventricle
The most common location of a cystic hygroma
The neck but may also be seen within the axilla
The most common sonographic appearance of pulmonary sequestration is
Triangular, echogenic mass with in the chest
Between the right ventricle in the right atrium, one should visualize the
Tricuspid valve
The most frequently encountered chromosomal abnormality associated with holoprosencephaly
Trisomy 13