Renal dysplasia-limb defects syndrome (RL syndrome), also known as Ulbright–Hodes syndrome, is a very rare autosomal recessive congenital disorder. It...

arthritis Renal dysplasia-limb defects syndrome Renfield syndrome Renpenning's syndrome Restless legs syndrome Restrictive dermopathy Retinoic acid syndrome Retirement...

organ abnormalities: cardiac defects (most frequently atrial septal defect and ventricular septal defects), and renal defects such as agenesis or multicystic...

Tracheoesophageal fistula E - Esophageal atresia R - Renal (Kidney) and/or radial anomalies L - Limb defects Although it was not conclusive whether VACTERL...

dysplasia other anomalies, also known as Cote Adamopoulos Pantelakis syndrome, Trichooculodermovertebral syndrome, TODV syndrome and Alves syndrome....

syndrome frequently manifests as pain when the limb is dependent (hanging down the edge of a bed/chair) and/or significant swelling of the whole limb...

issues such as hip dysplasia. The severity of repeated joint dislocations may lead to a differential diagnosis of Larsen syndrome, as suggested in one...

Esophageal atresia R — Renal (Kidney) and/or radial anomalies L — Limb defects Ventricular septal defect (VSD), atrial septal defects (ASD), and tetralogy...

tract include renal parenchyma, kidneys, and urinary collecting system. Defects can be bilateral or unilateral, and different defects often coexist in...

bilateral renal agenesis in 21.25% of cases; cystic dysplasia in 47.5%; obstructive uropathy in 25%; and others in 5.25%. Bilateral renal agenesis has...

setting of acute compartment syndrome, an urgent fasciotomy is warranted to protect the limb. Superior vena cava syndrome is a rare complication of arm...

Capillary leak syndrome, or vascular leak syndrome, is characterized by the escape of blood plasma through capillary walls, from the blood circulatory...

Ectrodactyly–ectodermal dysplasia–cleft syndrome, or EEC, and also referred to as EEC syndrome and split hand–split foot–ectodermal dysplasia–cleft syndrome: 520  is...

Meckel-Gruber syndrome is a rare, lethal ciliopathic genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations (occipital...

preferred agent, as warfarin is teratogenic (associated with birth defects). Budd Chiari syndrome in pregnancy is associated with an increased risk of miscarriage...

non-heritable birth defects via a toxic effect on an embryo or fetus. Defects include malformations, disruptions, deformations, and dysplasia that may cause...

Life-Threatening Rupture of an Intraparenchymal Aneurysm of Renal Artery (Wunderlich's Syndrome)". Case Reports in Vascular Medicine. 2013: 452317. doi:10...

investigation is done Abdominal wall defects are common in newborns with BWS and may require surgical treatment. These defects can range in severity from omphalocele...

cases of limb fusion correlate with more severe dysplasia in the pelvis. Rather than the two iliac arteries present in fetuses with complete renal agenesis...

(1991). "Retinal dysplasia in the Samoyed dog is the heterozygous phenotype of the gene (drds) for short limbed dwarfism and ocular defects". Transactions...

diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities". Molecular Cytogenetics. 12 (1): 19. doi:10...

Robinow syndrome is an extremely rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia...

bones or of the eye sockets (lambdoid suture defects, sphenoid dysplasia) Unilateral overgrowth of a limb. When a plexiform neurofibroma manifests on a...

cirrhosis, diverticulitis or cholangiocarcinoma. Renal vein thrombosis is the obstruction of the renal vein by a thrombus. This tends to lead to reduced...

females. Campomelic dysplasia – a condition caused by de novo autosomal dominant mutations in the SOX9 gene, causing bowing of the limbs, sex reversal in...

Hay–Wells syndrome (AEC syndrome, ankyloblepharon filiforme adnatum–ectodermal dysplasia–cleft palate syndrome, ankyloblepharon–ectodermal defects–cleft lip...

Simpson–Golabi–Behmel syndrome (SGBS) is a rare inherited congenital disorder that can cause craniofacial, skeletal, vascular, cardiac, and renal abnormalities...

brachydactyly, peculiar faces, hypoplastic epiglottis, cardiovascular defects, renal cysts, and also genital anomalies. Death occurs before or at birth.[citation...

Bilateral multicystic dysplastic kidneys Camptomelic dysplasia Cardiac rhabdomyoma Caudal regression syndrome Chorioangioma Cleft palate Club foot Coarctation...

examination showed Dandy–Walker malformation, ventricular septal defect, and renal cystic dysplasia. Cunniff et al. (1990) described affected brothers and 3 other...