Chater 26 The Fetal Spine And Musculoskeletal System Flashcards
Diagnosis of clubfoot?
The metatarsals and toes lie in the same plane as the tibia and fibula
What condition is associated with bilateral renal agenesis, olihydramnios, and fusion of the lower extremities?
Sirenomelia
A protein produced by the yolk sac and fetal liver that is found in excess in the maternal circulation in the presence of NTD is:
AFP
What term is defined as fusion of the digits?
Syndactyly
A cloverleaf skull and hydrocephalus is seen with:
Thanatophoric dysplasia
Sonographically, you visualize a mass extending from the distal spine of a fetus. The mass could be:
*SCT
*Meningocele
*Meningomyelocele
Absence of the radius is referred to as:
Radial Ray defect
Sirenomelia is commonly referred to as:
Mermaid syndrome
The exaggerated distance between the first toe and the second toe is:
Sandal Gap
What is associated with amniotic band syndrome:
*Amputation of fetal parts
*Anencephaly
*Facial clefting
Signs of Arnold-Chiari II malformation:
*Banana sign
*Lemon sign
*Colpocephaly
A bell-shaped chest and multiple fetal fractures are indicative of:
Osteogenesis imperfecta
Characteristic sonographic findings of achondrogenesis:
*Micromelia
*Absent mineralization of the pelvis
*Polyhydraminos
Absent long bones with the hands and feet arising from the shoulders and hips describes:
Phocomelia
An absent sacrum and coccyx is referred to as:
Caudal regression syndrome
Rhizomelia denotes:
Shortening of the proximal segment of a limb
The thalamic tissue located within the third ventricle of the brain that can become enlarged with Arnold-Chiari II malformation is:
Massa intermedia
What abnormality results in limitation of the fetal limbs as a result of joint contractures?
Arthrogryposis
Achondroplasia is associated with:
*Frontal bossing
*Flattened nasal bridge
*Trident hand
The most common nonlethal skeletal dysplasia is:
Achondroplasia
In VACTERL association, the letter “L” stands for
Limb
The group of fetal head and brain abnormalities that often coexists with spina bifida is referred to as:
Arnold-Chiari II malformation
______would increase the likelihood of a fetus developing sirenomelia and caudal regression syndrome
Preexisting maternal diabetes
A disorder that results in abnormal bone growth and dwarfism is:
Achondroplasia
What are clinical or sonographic findings consistent with LBWC:
*Ventral wall defects
*Marked scoliosis
*Shortened umbilical cord
The lemon sign denotes:
An abnormal shape of the fetal skull
The abnormal lateral curvature of the spine is referred to as:
Scoliosis
In VACTERL association, the letter “C” stands for:
Cardiac
Characteristics of spina bifida cystica:
*Banana sign
*Lemon sign
*Enlarged massa intermedia
The abnormal lateral ventricle shape in which there is a small frontal horn and enlarged occipital horn is referred to as:
Colpocephaly
Characteristics of spina bifida occulta:
*Closed defect
*Sacral dimple
*Hemangioma
The condition associated with the absence of the sacrum and coccyx:
Caudal regression syndrome
The form of inheritance in which at least one parent has to be a carrier of an abnormal gene for it to be passed to the fetus is:
Autosomal dominant