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376 Possible Causes for Severe Postnatal Growth Retardation

  • Cockayne Syndrome

    They exhibit intrauterine growth retardation, poor postnatal growth, severe and more rapidly progressive neurological impairment.[ijpd.in] Our patient had intrauterine growth retardation, a little postnatal neurologic development, a severe clinical form of Cockayne syndrome.[latunisiemedicale.com] , moderate pre- and postnatal growth retardation, and the absence of major malformations; and type iii in which phenotypic manifestations are related to chromosomal aneuploidies[icd10data.com]

  • Microcephalic Osteodysplastic Primordial Dwarfism Type II

    ), severe postnatal growth retardation, short stature, skeletal abnormalities and an unusually small head size and blood vessel abnormalities; A number of affected individuals[oatext.com] Microcephalic osteodysplastic primordial dwarfism type II is a specific disorder characterized by severe intrauterine and postnatal growth retardation, acquired microcephaly[ncbi.nlm.nih.gov] The classic features of the MPD group are severe pre- and postnatal growth retardation, with marked microcephaly.[ncbi.nlm.nih.gov]

  • Sanjad-Sakati Syndrome

    The main feature of Kenny-Caffey syndrome type 1 and 2 (KCS1, OMIM phenotype number #244460 ; KSC2, OMIM phenotype number #127000 ) is a bone dysplasia with severe postnatal[iofbonehealth.org] It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth retardation, dysmorphic features, as well as mild to severe mental retardation.[ingentaconnect.com] It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth retardation, and distinct facial dysmorphism.[ncbi.nlm.nih.gov]

  • Growth Failure

    ), severe postnatal growth retardation, short stature, skeletal abnormalities and an unusually small head size and blood vessel abnormalities; A number of affected individuals[oatext.com] In this report, we describe a 15-year-old boy with severe prenatal and postnatal growth failure, sensorineural deafness, and mental retardation who had a homozygous partial[nejm.org] , but severe postnatal growth failure, commencing within the first few months of life.[oncohemakey.com]

  • Russell-Silver Syndrome

    Russell-Silver Syndrome (RSS) is a genetically determined condition characterized by severe intrauterine and postnatal growth retardation; relative macrocephaly; a small,[ncbi.nlm.nih.gov] Silver-Russell syndrome (SRS) is a clinically and genetically heterogeneous condition characterised by severe intrauterine and postnatal growth retardation.[ncbi.nlm.nih.gov] RSS is characterized by severe intrauterine growth retardation, postnatal short stature, asymmetry of the face, body, and limbs, short and incurved fifth fingers, broad forehead[ncbi.nlm.nih.gov]

  • Seckel Syndrome

    The syndrome is characterized by severe intrauterine and postnatal growth retardation with proportional dwarfism, typical beak-like triangular nose, and mental retardation[ncbi.nlm.nih.gov] - and postnatal growth retardation, 2) microcephaly with mental retardation, and 3) specific dysmorphic features.[ncbi.nlm.nih.gov] Seckel syndrome (SS) is a rare, autosomal recessive syndrome; characterized by severe intrauterine and postnatal growth retardation, microcephaly, mental retardation, and[ncbi.nlm.nih.gov]

  • Costello Syndrome

    The typical clinical traits include dysmorphic craniofacial features, skin hyperpigmentation and excess, feeding difficulties leading to severe postnatal growth retardation[ncbi.nlm.nih.gov] […] feeding difficulties, failure to thrive, mild to severe intellectual disability, severe postnatal growth retardation, cardiac abnormalities or cancer predisposition.[ncbi.nlm.nih.gov] June 2017 Costello syndrome (CS) is a rare multiple congenital disorder caused by activating germline mutations in HRAS gene and is characterised by coarse facial features, severe[institut-myologie.org]

  • Cerebro-Oculo-Facio-Skeletal Syndrome Type 1

    growth retardation, severe psychomotor retardation, cerebral and cerebellar degeneration with calcification in basal ganglia and white matter, progressive joint contractures[medlink.com] They also exhibit a predominantly postnatal growth failure, a severe psychomotor retardation, with axial hypotonia and peripheral hypertonia and neonatal feeding difficulties[ncbi.nlm.nih.gov] growth retardation, severe psychomotor retardation, microcephaly with cerebral and cerebellar degeneration and calcification in basal ganglia and white matter, arthrogryposis[medlink.com]

  • 3M Syndrome Type 1

    Definition An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence[uniprot.org] The 3M syndrome is a rare autosomal recessive disorder recently ascribed to mutations in the CUL7 gene and characterized by severe pre- and postnatal growth retardation.[ncbi.nlm.nih.gov] Abstract The 3M syndrome is a rare autosomal recessive disorder recently ascribed to mutations in the CUL7 gene and characterized by severe pre- and postnatal growth retardation[ncbi.nlm.nih.gov]

  • Laron Syndrome

    It is characterized by severe postnatal growth retardation and characteristic facial features as well as high circulating levels of growth hormone (GH) and low levels of insulin-like[ncbi.nlm.nih.gov] Homozygous GHR/BP knockout mice showed severe postnatal growth retardation, proportionate dwarfism, absence of the GHR and GH binding protein, greatly decreased serum insulin-like[ncbi.nlm.nih.gov] Salient features shared between the two species are the absence of the GHR and GHBP, the severe postnatal growth failure, delayed puberty, and low IGF-I and elevated GH levels[ncbi.nlm.nih.gov]

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