Summer Sono 2011
Quiz yourself by thinking what should be in
each of the black spaces below before clicking
on it to display the answer.
Help!
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| CLEFT LIP | THE MOST COMMON FACIAL ANOMALY
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| CYSTIC HYGROMA | MOST COMMON NECK ANOMALY
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| CRANIOSYNOSTOSIS | PREMATURE OSSIFICATION OF SUTURES OF THE HEAD
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| HEMIFACIAL MICROSOMIA | ONE SIDE OF FACE IS SMALL AND EAR SET LOW
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| MANDIBLE | LARGE U SHAPE BONE CONSTITUTING THE LOWER JAW, CONTAINS LOWER TEETH
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| MECKEL GRUBER SYNDROME | LETHAL CONDITION ASSO W ENCEPHALOCELE
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| MEDIAN CLEFT FACE | WIDE SEPARATION OF NASAL ELEMENTS, POSSIBLE CLEFTING
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| MICROGNATHIA | SMALL CHIN / MANDIBLE
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| OTOCEPHALY | ABSENT MANDIBLE EARS CLOSE TOGETHER ANT TOWARD NECK
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| 5 WEEKS | THE CNS BEGINS TO FORM
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| 6 WEEKS | THE SUPERIOR PORTION OF THE FETUS ELONGATES TO FORM THE BRAIN.
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| 10-11 WEEKS | MINERALIZATION OF THE BONES
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| 18 WEEKS | CEREBELLAR VERMIS DEVELOPS
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| 18-20 WEEKS | CORPUS CALLOSUM DEVELOPS
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| 7 WK | LIMB BUDS DEVELOP
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| 8 WK | OSTEOGENESIS BEGINS IN CLAVICLE & MANDIBLE
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| 11-12 WKS | PRIMARY OSSIFICATION CENTERS OF LONG BONES ARE IDENTIFIED
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| 4TH MTH | ISCHIUM, METACARPALS OSSIFY
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| 5TH-6TH MTH | PUBIS, CALCANEUS OSSIFY
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| CAUDAL REGRESSION | PARTIAL TO COMPLETE SACRAL AGENESIS AND ABNORMALITIES OF THE LUMBAR SPINE, PELVIS, AND LOWER LIMBS
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| THANATOPHORIC DYSPLASIA TYPE I | TYPICAL “TELEPHONE RECEIVER” SHAPE OF THE EXTREMITIES; FRONTAL BOSSING; CRANIOSYNOSTOSIS; PLATYSPONDYLY
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| ACHONDROGENESIS | 2ND MOST COMMON LETHAL SKELETAL DYSPLASIA
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| ACHONDROGENESIS TYPE I | 20%; SHORT, CUBOID BONES; METAPHYSEAL SCALLOPING; AUTOSOMAL RECESSIVE; THICK, REDUNDANT SKIN FOLDS
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| OSTEOGENESIS IMPERFECTA TYPE II | THE NEONATAL LETHAL FORM OF SKELETAL DYSPLASIA
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| HYPOPHOSPHATASIA CONGENITAL | LETHAL; 1:100,000; THIN APPEARANCE OF BONES
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| CAMPTOMELIC DYSPLASIA | SHORT AND VENTRALLY BOWED TIBIA AND FEMUR; ABSENT OR HYPOPLASTIC FIBULA
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| SHORT-RIB POLYDACTYLY SYNDROME | DECREASED THORACIC CIRCUMFERENCE; POLYDACTYLY; GENITOURINARY ABNORMALITIES
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| HETEROZYGOUS ACHONDROPLASIA | BRACHYDACTYLY, WITH A TRIDENT CONFIGURATION OF THE HAND
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| ASPHYXIATING THORACIC DYSPLASIA | INVERTED “HANDLEBAR” APPEARANCE OF THE CLAVICLES, POLYDACTYLY
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| ELLIS-VAN CREVELD SYNDROME | HIGH PREVALENCE AMONG INBRED POPULATIONS
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| OSTEOGENESIS IMPERFECT TYPE I | BLUE SCLERAE; MOST FRACTURES OCCUR FROM CHILDHOOD TO PUBERTY; PROGRESSIVE HEARING LOSS
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| OSTEOGENESIS IMPERFECT TYPE III | NONLETHAL; PROGRESSIVELY DEFORMING VARIETY THAT OFTEN SPARES THE HUMERI, VERTEBRAE, AND PELVIS
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| PROXIMAL FOCAL FEMORAL DEFICIENCY | ASYMMETRICAL DEGREE OF ABSENCE OF SUBTROCHANTERIC FEMUR; IPSILATERAL FIBULAR HEMIMELIA
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| RADIAL RAY DEFECTS | ABSENCE OF A VISUALIZED FOREARM BONE, ASSOCIATED WITH TALIPOMANUS (CLUB HAND)
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| AASE SYNDROME | HYPOPLASTIC DISTAL RADIUS WITH RADIAL CLUBHAND, AND A TRIPHALANGEAL THUMB; CARDIAC DEFECTS
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| ARTHROGRYPOSIS MULTIPLEX CONGENITAL | MULTIPLE JOINT CONTRACTURES; LIMB PTERYGIUM; “BUDDHA POSITION” OF THE FETUS
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| DECIDUA BASALIS | THICK DECIDUA AT IMPLANTATION SITE
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| DECIDUA CAPSULARIS | THIN, OVERLIES GS FACING UTERINE CAVITY
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| CHORION FRONDOSUM | PORTION OF CHORION AT IMPLANTATION SITE
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| CHORIONIC VILLI | FUNCTIONING UNITS OF PLACENTA
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| COTYLEDONS | COMPOSED OF SEVERAL VILLI AND THEIR BRANCHES
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| RETROPLACENTAL COMPLEX | COMPOSED OF MYOMETRIUM, PLACENTA, AND VESSELS
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| FETAL SURFACE OF PLACENTA | CHORIONIC PLATE
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| BASAL PLATE | DIVIDED INTO COTYLEDONS(COMPOSED OF SEVERAL VILLI & THEIR BRANCHES)
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Created by:
amitamura
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