anencephaly/edema

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Adrenal cytomegaly is a frequent pathologic finding in hemoglobin bart hydrops fetalis.

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Adrenocortical cytomegaly (AC) is a relatively uncommon phenomenon but tends to occur in certain situations, including specific congenital anomalies and hydrops due to maternal-fetal Rhesus incompatibility. Because the pathology in the latter condition does not differ greatly from hemoglobin (Hb)

Temporal bone studies in anencephaly.

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The principal anatomical and histological features of the temporal bones of three anencephalics are described, one a twin-headed monster, with four temporal bones. These may be summarized as follows: Malformation of ossicles. Mondini type malformation of the cochlea. Occasionally cochlear hydrops or

A morphometric study of normal and abnormal fetal to childhood tongue size.

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The weight, length, width and thickness of 83 normal tongues from patients aged 25 weeks of gestation to 10.5 years were compared statistically with several measures of body and head size and changes described by linear regression; the relationships between measures were examined by partial and

Ultrasound in fetal diagnosis and therapy.

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Ultrasonic diagnosis is indispensable in perinatal medicine. The applications are; 1) diagnosis of early pregnancy, 2) diagnosis of fetal life, 3) diagnosis of pregnancy weeks by fetal crown rump length, 4) evaluation of fetal growth by biparietal diameter, femur length, abdominal size, or estimated

Prenatal ultrasonic detection of anomalies with a lethal or disastrous outcome.

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Although rare, a number of fetal anomalies can be detected with ultrasound in which the prognosis is either fetal death or minimal development. Anomalies of this type include anencephaly, holoprosencephaly, hydranencephaly, iniencephaly, cystic hygroma with hydrops, cystadenomatoid malformation of

Iniencephaly and chromosome mosaicism: a report of two cases.

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We report here two iniencephaly fetuses with chromosome mosaicism. The first fetus (22 weeks) was male with mosaic trisomy 13, and the second fetus (24 weeks) was female with mosaic monosomy X. The first fetus had anencephaly, facial clefting, left-sided rocker bottom foot, equinovarous deformity,

Correlation between ultrasound and autopsy findings after 2nd trimester terminations of pregnancy.

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OBJECTIVE To compare ultrasound (US) and fetal autopsy findings in 2(nd) trimester termination of pregnancy because of structural fetal anomalies. METHODS A total of 112 terminations of pregnancy (TOP) between 1999-2003 were reviewed retrospectively. The cases originated from a secondary and a

Usefulness of antenatal ultrasound fetal morphological assessments in the first and second trimester: a study at a single Japanese university hospital.

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OBJECTIVE To assess the usefulness of antenatal ultrasound examinations for detecting fetal morphological abnormalities in the first and second trimesters. METHODS A prospective cohort study was conducted at a single Japanese university hospital in the period from February 2011 to September 2013.

Congenital malformation in newborns. Analysis of 501 cases.

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Over a 14-year period in Chang Gung Memorial Hospital, 510 out of 44, 362 newborns were found to have birth defects. Maternal age, gestational age, parity, infant sex and birth weight were analyzed for each anomaly and compared to normal newborns. The average maternal age and parity for newborns

[Color and duplex Dopplerometry in the prenatal diagnosis of congenital developmental defects].

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OBJECTIVE Impact of Doppler system in detection of congenital malformations during prenatal diagnosis. METHODS Prospective clinical study. METHODS Department of Medical Genetics and Foetal Medicine, Department of Obstetrics and Gynaecology University Hospital Olomouc. METHODS In 34 pregnancies with

Postnatal outcome of congenital anomalies in low resource setting.

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OBJECTIVE This study aimed to determine the postnatal outcome of congenital malformations in a tertiary care hospital of India. METHODS This was a prospective study of all women with prenatally detected major congenital malformations. Postnatal follow-up of live born babies was carried out for 1

A study of fetal anomalies detected by ultrasound in Bangladesh and their relative frequencies.

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A total of 5,841 obstetric patients were scanned over a period of 34 months. This study was undertaken to establish the anomalies that can be detected by ultrasound and to find out their relative frequencies in Bangladesh. Of the 41 cases of congenital anomalies, seven cases were of hydrocephalus,

Detection of fetal structural abnormalities by an 11-14-week ultrasound dating scan in an unselected Swedish population.

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BACKGROUND To determine the detection rate of fetal structural abnormalities by a routine 11-14-week ultrasound scan for dating in an unselected pregnant population. METHODS A prospective observational cohort study of 2,708 unselected pregnant women attending an abdominal ultrasound examination at

Early ultrasound diagnosis of Neu-Laxova syndrome.

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We report the mid-trimester prenatal diagnosis of Neu-Laxova syndrome (NLS) in two at risk families utilizing serial sonographic examinations. Ultrasound and pathologic findings from seven affected pregnancies, the largest case series of NLS to date, are presented. One fetus had anencephaly and

Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound.

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OBJECTIVE To design a scheme to rank sonographic anomalies as indicators of aneuploidy and record the distribution of data from 2143 prenatal amniotic fluid/chorionic villous sample diagnoses referred for karyotyping because of fetal anomalies detected with ultrasound. METHODS In all cases the

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