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593 Possible Causes for Hydronephrosis, prenatal and postnatal, Short Stature

  • Russell-Silver Syndrome

    Abstract A family is described with a syndrome of short stature, abnormal pigmentation of the skin and mild facial dysmorphism.[] Russell-Silver syndrome (RSS) should be suspected in patients with prenatal and postnatal growth retardation.[] […] cafe-au-lait marks) Curving of the pinky toward the ring finger Delayed bone age Failure to thrive Gastroesophageal reflux disease Kidney problems, such as: Horseshoe kidney, Hydronephrosis[]

  • Turner Syndrome

    stature (Short-Stature Group) were enrolled.[] Research Prenatal and postnatal...[] Silent hydronephrosis. Gonadal dysgenesis/failure Many have fibrotic ovarian streaks at the time of birth.[]

  • Robinow Syndrome

    We describe a child with short stature of prenatal onset, rhizomelic limb shortness affecting the upper limbs particularly, and an unusual face.[] The prenatal and postnatal findings, the differential diagnosis, and the prognosis of patients with this syndrome are discussed. 2013 Wiley Periodicals, Inc.[] Involvement of other organs and tissues has been recognized as well, examples being renal disease (hydronephrosis), congenital heart disease (bicuspid aortic valve, stenosis[]

  • Growth Failure

    Children with short stature in whom no specific cause is identified may be diagnosed with idiopathic short stature.[] Thus, while GH does not appear to be essential for intrauterine growth, IGF-I itself is critically involved in both prenatal and postnatal growth.[] Ultrasound of the abdomen revealed hydronephrosis of the left kidney and an absent right kidney.[]

  • XXXXY Syndrome

    Both boys are mentally retarded with short stature, muscular hypotonia, and hypogonadism.[] Mean height is typically below average, and growth deficiency is associated both prenatally and postnatally, which could be due to the extreme over- dosage of sex chromosome[] Abstract A 1-month-old boy was referred to our hospital with right hydronephrosis.[]

  • Wiedemann-Rautenstrauch Syndrome

    Patients have premature aging aspect, short stature and a poorly muscled build.[] She had prenatal and postnatal growth failure, generalized lipoatrophy except for fat pads in the suprabuttock areas, triangular face, pseudohydrocephalous, sparse scalp hair[] […] infiltration of liver Fatty liver [ more ] 0001397 Hip dysplasia 0001385 Hirsutism Excessive hairiness 0001007 Hydrocephalus Too much cerebrospinal fluid in the brain 0000238 Hydronephrosis[]

  • Raine Syndrome

    Our patient had the common craniofacial features as well as, uncommon features such as protruding tongue, short stature, and hypoplastic distal phalanges.[] Appositional new bone formation may be mistaken for fractures and callus formation--both prenatally by ultrasound and postnatally in radiographs.[] Extra-skeletal features can be hydronephrosis and ureteral stenosis. Etiology Mutations in the FAM20C gene have a causative role in lethal osteosclerotic bone dysplasia.[]

  • Trisomy 18

    Our first patient is an 8(1/2)-year-old female with normal intelligence and no significant dysmorphic features other than short stature and cubitus valgus.[] The purpose of this manuscript is to present a model for the care of fetuses and infants with trisomy 13 and 18 during the prenatal, perinatal, and postnatal periods.[] […] with involvement of the eyes (microphthalmia, coloboma), heart (over 90% of cases) digestive tract (esophageal atresia, anorectal malformations), kidneys and urinary tract (hydronephrosis[]

  • Congenital Malformation Syndromes Involving Early Overgrowth

    Describe when treatment is indicated for children with short and tall stature.[] In some of these cases, genetic analysis has indicated that the prenatal and postnatal growth retardation associated with Chromosome 15 Ring (and potentially suggestive of[] Symptoms List: 15q overgrowth syndrome Symptoms and clinical features may include: 1 Clinical Features of 15q overgrowth syndrome : Horseshoe kidney Hydronephrosis Bifid uvula[]

  • Sanjad-Sakati Syndrome

    Sanjad Sakati Syndrome /Dysmorphism/ short stature 30 Days of Hope: Day Nine #NICUphotography, #preemie, #NICU, #placentaprevia, #34weeks, #preemiesupportandawareness, #capturinghopes[] It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth retardation, and distinct facial dysmorphism.[] CT abdomen showed bilateral renal pelvic stones and mild hydroureter and hydronephrosis. The patient was then referred to the DEMPU clinic.[]

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