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742 Possible Causes for Failure to Thrive, Narrow Hands

  • Prader-Willi Syndrome

    […] and feet small for height/age Narrow hands with straight ulnar border Esotropia, myopia Thick, viscous saliva Speech articulation defects Skin picking Major criteria are[arupconsult.com] Prader-Willi syndrome (PWS) is characterized by infantile lethargy and hypotonia causing poor feeding and failure to thrive, childhood obesity, short stature, and hypogonadism[ncbi.nlm.nih.gov] The patient has hypotonia, failure to thrive, and typical dysmorphic facial features for PWS.[ncbi.nlm.nih.gov]

  • Hypertension

    In arterioles, on the other hand, decreases in the density of blood vessels (rarefaction) and in vasomotion amplitude may play a more important role than reductions in lumen[ncbi.nlm.nih.gov] Relevant information includes the following: Prematurity Bronchopulmonary dysplasia History of umbilical artery catheterization Failure to thrive History of head or abdominal[web.archive.org] Failure to thrive, seizures, irritability, lack of energy, and difficulty in breathing can be associated with hypertension in newborns and young infants.[en.wikipedia.org]

  • CAMFAK Syndrome

    […] palate Renal hypoplasia Joint contracture of the hand Trophic changes related to pain Respiratory insufficiency due to muscle weakness Poor suck Akinesia Scaphocephaly Fetal[mendelian.co] Diseases related to Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome via text searches within MalaCards or GeneCards Suite gene sharing: Human phenotypes[malacards.org] Research of Cataract, Microcephaly, Failure To Thrive, Kyphoscoliosis Syndrome has been linked to Microcephaly, Hereditary Diseases, Failure To Thrive, Peripheral Neuropathy[novusbio.com]

  • Marshall-Smith Syndrome

    Bullet-shaped middle finger bones 0009845 Cerebral atrophy Degeneration of cerebrum 0002059 Choanal stenosis Narrowing of the rear opening of the nasal cavity 0000452 Death[rarediseases.info.nih.gov] It is hoped that the etiology of the syndrome will be discovered as more cases are recognized and reported by pediatricians caring for infants with failure to thrive, advanced[ncbi.nlm.nih.gov] Marshall A syndrome of motor and mental retardation, accelerated skeletal maturation, failure to thrive, and abnormal facies.[whonamedit.com]

  • Smith Lemli Opitz Syndrome

    Other dysmorphic features may include microcephaly, ptosis, epicanthal folds, short nasal bridge, bitemporal narrowing, and micrognathia.[jneurodevdisorders.biomedcentral.com] Affected individuals have dysmorphism, short stature, failure to thrive, microcephaly, multiple congenital malformations, and mental retardation.[ncbi.nlm.nih.gov] We found correlations between multiple congenital malformations, failure to thrive and low plasmatic cholesterol measurement.[ncbi.nlm.nih.gov]

  • Sanjad-Sakati Syndrome

    Dysmorphism is most evident on the face, with the following features: Long narrow face Deep-set, small eyes Beaked nose Large, floppy ears Small head ( microcephaly ) and[en.wikipedia.org] We encountered a 2-year-old boy with hypocalcemia, failure to thrive and macrocytic anemia.[ncbi.nlm.nih.gov] […] marrow cavities of long bones Small hands and feet Calvarial osteosclerosis Medullary stenosis of tubular bones Small hands and feet Mental Mental retardation (mild to moderate[ncbi.nlm.nih.gov]

  • Alagille Syndrome

    Xanthomas can be found over knees, elbows, hands, and around the eyes. Heart defects – a heart murmur can be detected by doctors in patients with Alagille syndrome.[news-medical.net] Abstract A 4-year-old girl with failure to thrive and intense pruritus associated with Alagille syndrome is described.[ncbi.nlm.nih.gov] An 8-year old child with persisting jaundice, severe itching and failure to thrive.[ncbi.nlm.nih.gov]

  • Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome

    Small mouth 0000160 Rocker bottom foot Rocker bottom feet Rocker-bottom feet Rockerbottom feet [ more ] 0001838 1%-4% of people have these symptoms Joint contracture of the hand[rarediseases.info.nih.gov] Additional features include severe failure to thrive, platelet dysfunction (which may be responsible for severe bleeding), facial dysmorphism (low set ears, lax skin, a high[rarediseases.info.nih.gov] Additional features include ichthyosis, central nervous system malformation, platelet anomalies, and severe failure to thrive.[unboundmedicine.com]

  • Lenz-Majewski Syndrome

    0000885 Choanal stenosis Narrowing of the rear opening of the nasal cavity 0000452 Chordee 0000041 Cutis laxa Loose and inelastic skin 0000973 Cutis marmorata 0000965 Diaphyseal[rarediseases.info.nih.gov] The disorder is characterized by failure to thrive and mental retardation.[doi.org] […] to thrive, mental retardation, sparse hair, enamel hypoplasia, loose skin, and skeletal abnormalities.[accessanesthesiology.mhmedical.com]

  • Noonan Syndrome

    Poor muscle tone and lethargy Difficulty feeding Narrow forehead and almond-shaped eyes Puffy hands and fingers Abnormally increased appetite Lack of satiety after eating[norditropin.com] […] to thrive, short stature, feeding difficulties, sternal deformity, renal malformation, pubertal delay, cryptorchidism, developmental or behavioral problems, vision problems[ncbi.nlm.nih.gov] The patient presented with postnatal-onset failure-to-thrive, developmental delay, microcephaly, velopalatal incompetence, pectus excavatum, coarctation of aorta, atrial and[ncbi.nlm.nih.gov]

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