Anomalies of the Auditory Organ in Potter's Syndrome: Histopathological Findings in the Temporal Bone

Saito, Ryusuke; Takata, Nobuo; Matsumoto, Noriaki; Koide, Ikuo; Fujita, Akira; Ogura, Yuichiro; Murakami, Motomasa; Yanagida, Kohsuke; Komazawa, M

doi:10.1001/archotol.1982.00790560022006

Cited by 7 publications

(3 citation statements)

References 15 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Such an association was described in several studies [2,7,13,14]. Some of the studies found evidence of Mondini or Schiebe defect in a series of patients who were congenitally deaf and also had chronic congenital renal disease (nephritis) [2].…”

Section: Discussionmentioning

confidence: 73%

See 1 more Smart Citation

Recurrent meningitis and cerebrospinal fluid leak–two sides of the same vestibulocochlear defect: report of three cases

et al. 2006

View full text Add to dashboard Cite

show abstract

Section: Discussionmentioning

confidence: 73%

“…Some of the studies found evidence of Mondini or Schiebe defect in a series of patients who were congenitally deaf and also had chronic congenital renal disease (nephritis) [2]. Others described a familial branchio-oto-renal dysplasia [7,13] or anomalies of the auditory organ with renal agenesis as part of the Potter syndrome [14].…”

Section: Discussionmentioning

confidence: 99%

Recurrent meningitis and cerebrospinal fluid leak–two sides of the same vestibulocochlear defect: report of three cases

et al. 2006

View full text Add to dashboard Cite

show abstract

“…Potter concluded that area "A" was the most commonly affected. Embryonic area "B" was more extensive, including atresia of bladder and imperforate anus with atresia of the Davidson and Ross, 1954;Bain and Scott, 1960Potter, 1965Bergsma, 1979Potter, 1965Woolf and Allen, 1953Hilson, 1957Potter, 1965; Warkany , 197 1 ; Leonidas et al, 1982Saito et al, 1982Wright et al, 1981Potter, 1965Welch, 1958Potter, 1946Potter, 1965;Davidson and Ross, 1954;Kuhner et al, 1976;Potter, 1965Bergsma, 1979Potter, 1965Bergsma, 1979Potter, 1965Greenwood et al, 1976Hislop et al, 1979;Potter, 1965;Welch, 1958Bergsma, 1979Potter, 1965Potter, 1965Cote et al, 1978Yunis et al, 1980 aVentricular septal defect. hPatent ductus arteriosus.…”

Section: Associated Anomaliesmentioning

confidence: 99%

Renal agenesis in British Columbia

Wilson

Baird

1985

Am. J. Med. Genet.

View full text Add to dashboard Cite

We review the incidence of bilateral and unilateral renal agenesis occurring in more than 625,000 consecutive births in British Columbia from 1952 to 1982. In total, 92 cases of bilateral renal agenesis and 117 cases of unilateral renal agenesis were identified. Congenital anomalies occurring in association with these conditions were also analyzed. The findings of the study support a mechanism in at least a proportion of cases of a primary developmental defect involving multiple systems within the fetus, with oligohydramnios being the result of the syndrome not the cause. Oligohydramnios no doubt contributes to the anomalies of the face, musculoskeletal system, and genitalia. No trends in changing incidence over time were identified.

show abstract

The Potter sequence: A clinical analysis of 80 cases

et al. 1984

View full text Add to dashboard Cite

Eighty cases of Potter sequence due to a renal or urologic abnormality were studied retrospectively. The abnormal renal findings were bilateral renal agenesis in 21.25%; cystic dysplasia in 47.5%; obstructive uropathy in 25%; and others in 5.25%. Fifteen patients had multiple congenital anomalies; of these three had aneuploidy, four had autosomal recessive syndromes, and eight were of unknown cause. Results of chromosome analysis in 41 patients and 21 sets of parents were abnormal in three patients, one of whom had a balanced translocation carrier parent; two additional patients and three parents had apparently balanced translocations. There was one recurrence within the study (the first child had bilateral renal agenesis and the second cystic dysplasia). The ultrasound prenatal diagnosis of the renal abnormality was made in eight cases between 18 and 34 weeks. Family histories were suggestive of an autosomal dominant gene disorder with incomplete penetrance in four of 45 families with nonsyndromic bilateral renal agenesis and cystic dysplasia. The evaluation of patients with the Potter sequence should include an examination for nonrenal defects, autopsy, chromosome analysis, and renal ultrasound or urologic evaluation of parents. Ultrasonographic prenatal monitoring of subsequent pregnancies in such families is strongly warranted because of a definite but unknown degree of recurrence risk.

show abstract

Anomalies of the Auditory Organ in Potter's Syndrome: Histopathological Findings in the Temporal Bone

Cited by 7 publications

References 15 publications

Recurrent meningitis and cerebrospinal fluid leak–two sides of the same vestibulocochlear defect: report of three cases

Recurrent meningitis and cerebrospinal fluid leak–two sides of the same vestibulocochlear defect: report of three cases

Renal agenesis in British Columbia

The Potter sequence: A clinical analysis of 80 cases

Contact Info

Product

Resources

About