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4,173 Possible Causes for Failure to Thrive, Holoprosencephaly, Syndactyly between Adjacent Toes

  • Pallister-Hall Syndrome

    ) Syndactyly (abnormal "webbing" between, or fusing of, adjacent fingers and/or toes) Short limbs Dysplastic nails ( i.e., finger nails and toe nails that are flaky and poorly[] […] to thrive cyanosis regurgitation/reflux DIFFERENTIAL DIAGNOSIS laryngomalacia vocal cord paralysis laryngopharyngeal reflux disease neuromuscular swallowing disorder reactive[] The spectrum of these anomalies is wide, ranging from alobar holoprosencephaly to microforms, such as isolated single central medial incisive, or cleft palate.[]

  • Patau Syndrome

    Infants who survive to one year have severe complications including intellectual disability, seizures and failure to thrive.[] Alobar holoprosencephaly and Trisomy 13 (Patau syndrome). Autopsy and Case Reports, 3 (2), 5-10.[] Prognosis Trisomy 18 is associated with severe mental retardation and severe failure to thrive. 50% of patients die by one week of life, and 90% of patients die by one year[]

    Missing: Syndactyly between Adjacent Toes
  • Smith Lemli Opitz Syndrome

    Affected individuals have dysmorphism, short stature, failure to thrive, microcephaly, multiple congenital malformations, and mental retardation.[] The diagnosis of alobar holoprosencephaly was confirmed at 15 weeks of gestation, and cardiac and limb defects were also identified.[] We found correlations between multiple congenital malformations, failure to thrive and low plasmatic cholesterol measurement.[]

    Missing: Syndactyly between Adjacent Toes
  • Growth Failure

    Presentation on theme: "Faltering growth(failure to thrive)"— Presentation transcript: 1 Faltering growth(failure to thrive) refers to not only failure of growth(suboptimal[] ., cleft palate, septo-optic dysplasia, or holoprosencephaly).[] […] found were pituitary gland hypoplasia or aplasia, ectopic pituitary gland, septooptic dysplasia, isolated absence of septum pellucidum, stalk abnormalities, empty sella, and holoprosencephaly[]

    Missing: Syndactyly between Adjacent Toes
  • Septo-Optic Dysplasia

    Marshall-Smith syndrome is characterized by advanced bone age, failure to thrive, respiratory problems, dysmorphic facial features, and variable mental retardation.[] In lobar holoprosencephaly which is the least severe form of other holoprosencephalies (alobar and semilobar), there is always varying degrees of fusion of the two cerebral[] […] to thrive. 2 Optic Nerve Hypoplasia Optic nerve hypoplasia is always present in septo-optic dysplasia.[]

    Missing: Syndactyly between Adjacent Toes
  • Chromosome 18p Deletion Syndrome

    Clinical features include cleft lip and palate, intellectual disability, failure to thrive, congenital heart disease, hypertonia, micrognathia, short sternum, low set malformed[] We present prenatal diagnosis of a de novo distal 18p deletion involving 14.06Mb at 18p11.32–p11.21 by aCGH using uncultured amniocytes in a pregnancy with fetal holoprosencephaly[] MalaCards based summary : Chromosome 18p Deletion Syndrome, also known as de grouchy syndrome, is related to 18p deletion syndrome and alobar holoprosencephaly.[]

    Missing: Syndactyly between Adjacent Toes
  • Lissencephaly

    Symptoms of the disorder may include unusual facial appearance, difficulty swallowing, failure to thrive, muscle spasms, seizures, and severe psychomotor retardation.[] Types of Holoprosencephaly The most serious form is alobar holoprosencephaly, in which the hemispheres completely fail to separate.[] Convert to ICD-10-CM : 742.2 converts approximately to: 2015/16 ICD-10-CM Q04.1 Arhinencephaly Or: 2015/16 ICD-10-CM Q04.2 Holoprosencephaly Or: 2015/16 ICD-10-CM Q04.3 Other[]

    Missing: Syndactyly between Adjacent Toes
  • Monosomy 21q

    To Thrive Heredity Deletions Include Q11-1, Q11-1-Q22-1, Q11-2-Q21-3, Q21-1.2, Q22-1 And Q22-2 Nose Large Nose With A Broad Bridge And Epicanthic Folds Cardiovascular System[] Prenatal diagnosis of alobar holoprosencephaly, cyclopia, proboscis, and isochromosome 18q in the second trimester. AJP Rep. 2011;1:73–6.[] A malformed infant was delivered without the phenotype of holoprosencephaly (HPE).[]

    Missing: Syndactyly between Adjacent Toes
  • Erythroderma Desquamativum

    Blogs Submit your blog on Generalized Erythroderma, Diarrhea, And Failure To Thrive to be featured![] Hing Lambert-Eaton myasthenic type CDO syndrome Corneal dystrophy epithelial syndrome pavm Trisomy 17p Branchio-oculo-facial syndrome and short stature Lambotte syndrome holoprosencephaly[] Hyperphosphatasia Hermansky Pudlak syndrome Herpes, Neonatal Hers Disease Hiccups, Chronic Hidradenitis Suppurativa Hirschsprung's Disease Histidinemia Hodgkin's Disease Holoprosencephaly[]

    Missing: Syndactyly between Adjacent Toes
  • Craniosynostosis Type 3

    Examples of these defects include hydrocephalus, holoprosencephaly, multicystic renal dysplasia and severe hydrops.[] ., holoprosencephaly, microcephaly, shunted hydrocephalus, encephalocele) Exposure of fetus (e.g., valproic acid, phenytoin) Mucopolysaccharidosis (e.g., Hurler’s syndrome[] Hematologic disorders Congenital hemolytic icterus Polycythemia vera Sickle cell anemia Thalassemia Iatrogenic disorders Hydrocephalus with shunt Malformations Encephalocele Holoprosencephaly[]

    Missing: Failure to Thrive

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