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61 Possible Causes for Failure to Thrive, Prenatal and Postnatal Short Stature

  • Russell-Silver Syndrome

    Systematic testing of cases suspected prenatally or postnatally would be informative regarding the individual contribution of each factor.[ncbi.nlm.nih.gov] Russell-Silver syndrome is characterized by asymmetric intrauterine growth retardation, postnatal failure to thrive, distinct facial features, limb asymmetry, excessive sweating[ncbi.nlm.nih.gov] Mosaic trisomy 7 was diagnosed after birth, on fibroblasts karyotype performed for blaschkolinear pigmentary skin anomalies and failure to thrive.[ncbi.nlm.nih.gov]

  • Wolf-Hirschhorn Syndrome

    Short stature and slow weight gain is common postnatally. Central nervous system Neurologic concerns are common and include the following.[emedicine.medscape.com] Accordingly, prenatal-onset growth retardation and failure to thrive have been found to result from haploinsufficiency for a 4p gene located between 0.4 and 1.3 Mb, whereas[ncbi.nlm.nih.gov] Clinical manifestations of WHS include intrauterine growth restriction, failure to thrive in the neonatal period that is present simultaneously with hypotonia, typical "Greek[ncbi.nlm.nih.gov]

  • Familial Short Stature

    short stature.[ncbi.nlm.nih.gov] […] to thrive (child) R62.52 Short stature (child) R62.59 Other lack of expected normal physiological development in childhood R62.7 Adult failure to thrive R63 Symptoms and[icd10data.com] Clinical abnormalities include severe prenatal and postnatal growth failure and facial dysmorphism.[ncbi.nlm.nih.gov]

  • Hypophosphatasia

    […] teeth Clinical course, radiographs, laboratory findings Childhood (juvenile) AR or AD Short stature, skeletal deformity, bone pain/fractures Premature loss, deciduous teeth[ncbi.nlm.nih.gov] The infantile case presented with failure to thrive, hypotonia, and radiologic rickets at 4 months old.[ncbi.nlm.nih.gov] A 1-month-old boy visited the clinic because of poor feeding, frequent vomiting, hypotonia, and failure to thrive from birth.[ncbi.nlm.nih.gov]

  • Kenny-Caffey Syndrome Type 1

    […] and postnatal growth retardation, short stature, cortical thickening and medullary stenosis of the long bones, absent diploic space in the skull bones, hypocalcemia due to[malacards.org] CASE REPORT A 7-month-old girl was admitted to the children hospital in Damascus for the first time complaining of failure to thrive.[ncbi.nlm.nih.gov] Orpha Number: 93324 Disease definition A rare, primary bone dysplasia characterized by prenatal and postnatal growth retardation, short stature , cortical thickening and medullary[rarediseases.info.nih.gov]

  • Kaufman Oculocerebrofacial Syndrome

    Symptoms INHERITANCE: Autosomal recessive GROWTH: [Height]; Short stature, proportionate; [Weight]; Average birth weight 1540g; [Other]; Prenatal growth retardation; Postnatal[findzebra.com] thrive, eye abnormalities, other congenital malformations, low cholesterol levels, and severe intellectual disability.[ncbi.nlm.nih.gov] […] to thrive / difficulties for feeding in infancy / growth delay - High vaulted / narrow palate - Long face - Macrostomia / big mouth - Microcornea - Muscle weakness / flaccidity[csbg.cnb.csic.es]

  • Skeletal Dysplasia

    When presented with a patient that may have a skeletal dysplasia, the following must be performed: (a) Clinical evaluation: assessment of disproportionate short stature (prenatal[analesdepediatria.org] In addition, he presented with very severe prenatal growth failure, respiratory distress as a neonate, subsequent failure to thrive and susceptibility to airway infection,[ncbi.nlm.nih.gov] Hadju-Cheney syndrome (OMIM 102500 ) is characterized by short stature, failure to thrive, conductive hearing loss, dysmorphic features, early tooth loss, genitourinary anomalies[ncbi.nlm.nih.gov]

  • Bloom Syndrome

    These patients often have prenatal or postnatal growth retardation, short stature, malar hypoplasia, telangiectatic erythema of the face and other regions, hypo- and hyperpigmentation[mayomedicallaboratories.com] […] to thrive in infancy Very short stature Very small head Skin telangiectasias (spidery veins visible near the surface of the skin) Café au lait spots on the skin (see photo[forgottendiseases.org] […] to thrive was noted.[jmedicalcasereports.biomedcentral.com]

  • Cutis Laxa

    Severe short stature, mental retardation and hypertrophic cardiomyopathy are other associated manifestations (16).[caribbean.scielo.org] […] to thrive, developmental delay, dysmorphism, osseous abnormality, and CNS manifestations.[ncbi.nlm.nih.gov] Features of our patient that have been described in literature included cutis laxa on hands and feet, visible veins on thorax and abdomen, joint laxity, failure to thrive,[ncbi.nlm.nih.gov]

  • Turner Syndrome

    […] counseling and management after the diagnosis was made either prenatally or postnatally.[pediatrics.aappublications.org] […] to thrive in infancy Faltering weight in infancy Weight faltering in infancy [ more ] 0001531 Genu valgum Knock knees 0002857 Hashimoto thyroiditis 0000872 Hearing impairment[rarediseases.info.nih.gov] […] to thrive.[medicalhomeportal.org]

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