Closed bladder exstrophy (pseudoexstrophy) associated with mesodermal anomalies.

R O'Leary; P Davies; D Challis; G Bury

doi:10.7863/jum.1995.14.4.311

Home/Archive/PubMed

PubMed · 7602692

Closed bladder exstrophy (pseudoexstrophy) associated with mesodermal anomalies.

R O'Leary·P Davies·D Challis·G Bury

View original source ↗Export metadata ↓

Abstract

The source did not provide an abstract. Follow the original record for more information.

Explore related subjects

Abnormalities, Multiple Abortion, Therapeutic Adult Bladder Exstrophy Female Fetal Diseases Forearm Humans Mesoderm Musculoskeletal Abnormalities Musculoskeletal System Pregnancy Radiography Ultrasonography, Prenatal Urinary Bladder Case Reports Journal Article

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

R O'Leary, P Davies, D Challis, G Bury. 1995. Closed bladder exstrophy (pseudoexstrophy) associated with mesodermal anomalies.. https://doi.org/10.7863/jum.1995.14.4.311

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

PubMed1999

Carey-Fineman-Ziter (CFZ) syndrome: report on affected sibs.

We describe a sib pair with craniofacial anomalies, micrognathia, Mobius sequence, generalised myopathy, relative macrocephaly, and developmental delay. They appear to have the Carey-Fineman-Ziter syndrome (MIM 254940), which has been reported in only four children, a sib pair and two sporadic cases. This report on an additional affected brother and sister pair supports autosomal inheritance as the likely cause. These cases also confirm that scoliosis, talipes equinovarus, and a non-specific primary myopathy are important manifestations of Carey-Fineman-Ziter syndrome.

Abnormalities, Multiple↗

PubMed1999

Sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts: a new syndrome?

We describe two sib fetuses with situs inversus, cystic dysplastic kidney and pancreas, bowing of the lower limbs and clavicles, severe intrauterine growth retardation (IUGR), and oligohydramnios. Early prenatal diagnosis of pancreatic and dysplastic renal cysts and situs inversus totalis were made in the 18-week-old fetus. This syndrome differs from that of Ivemark and related syndromes because of the presence of situs inversus totalis and absence of hepatic fibrosis and cysts. The parents were first cousins, and did not have any cysts of kidney, liver, or pancreas detected by ultrasonography.

Abnormalities, Multiple↗

PubMed1999

Costello syndrome: report and review.

We describe a 34-year-old woman with mental retardation, short stature, macrocephaly, a "coarse" face, hoarse voice, and redundant skin with deep palmar and plantar creases who had evident Costello syndrome. Lacking papillomata, she had wart-like lesions of the skin. The previously reported patients with Costello syndrome are reviewed. Costello syndrome is probably an autosomal dominant disorder, either caused by a mutation in a single gene or by microdeletion.

Abnormalities, Multiple↗