Two fetuses with Fryns syndrome without diaphragmatic defects.
نویسندگان
چکیده
We report two fetuses with Fryns syndrome including the typical facial appearance and distal limb and lung hypoplasia, but no diaphragmatic hernias. The parents were consanguineous. Characteristic in both cases were the distal limb defects with brachytelephalangism and aplasia of the distal phalanges of the first toe. Since one of the two sibs had severe lung hypoplasia without macroscopic or microscopic defects of the diaphragm, we show that lung hypoplasia can occur independently from diaphragmatic defects in Fryns syndrome.
منابع مشابه
Cardiovascular malformations in Fryns Syndrome A case report
Fryns syndrome is characterized by multiple congenital anomalies including congenital diaphragmatic hernia (CDH), and congenital heart disease (CHD).The prognosis of infant with Fryns syndrome and left sided CDH when associated with pulmonary hypoplasia is grave. We report a 2year old boy with Fryns syndrome who had right sided CDH, Tetralogy of Fallot, and other multiple congenital anomalies. ...
متن کاملAtypical Fryns syndrome: clinical, radiological and pathological findings.
Fryns syndrome is an autosomal recessive hereditary disease, including abnormal facies, small thorax with widely spaced hypoplastic nipples, distal limb and nail hypoplasia, and diaphragmatic hernia with pulmonary hypoplasia. The aim of the present report is to increase awareness of Fryns syndrome and its association with rare abnormalities such as cecal duplication cyst, horseshoe kidney and b...
متن کاملSyndrome of the month
The name Fryns syndrome was given by Lubinsky et all to "a new variable multiple congenital anomaly syndrome" reported by us in 1979.2 We first detected this syndrome in two female sibs who presented with cloudy corneae, diaphragmatic defects, and distal limb deformities.2 The parents were unrelated and normal and chromosome investigation showed normal karyotypes in the parents and in one child...
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Congenital diaphragmatic hernia (CDH) is often associated with major anomalies and chromosomal abnormalities. Chromosomal abnormalities are usually detected in 9.5% to 34% of fetuses with CDH prenatally diagnosed and the defect has also been reported in association with multiple syndromes such as Pallister-Killian syndrome, Fryns syndrome, Di George syndrome and Apert syndrome. Among the chromo...
متن کاملCoexistence of congenital diaphragmatic hernia and abdominal wall closure defect with chromosomal abnormality: two case reports
BACKGROUND We reported two rare cases of congenital diaphragmatic hernia with abdominal wall closure defect, which were not associated with septum transversum diaphragmatic defects or Fryns syndrome. CASE PRESENTATION Case 1: a Japanese baby boy was delivered at 37 weeks' gestation by urgent cesarean section because of the diagnosis of severe fetal distress. Congenital diaphragmatic hernia wi...
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ورودعنوان ژورنال:
- Journal of medical genetics
دوره 31 12 شماره
صفحات -
تاریخ انتشار 1994