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13 Possible Causes for Failure to Thrive, Mild Maxillary Prognathism

  • Baller-Gerold Syndrome

    […] of the radius 0006501 Aplasia/Hypoplasia of the thumb Absent/small thumb Absent/underdeveloped thumb [ more ] 0009601 Brachyturricephaly High, prominent forehead 0000244 Failure[rarediseases.info.nih.gov] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] At an older age (patient 4 at 3 and 6 years), dysmorphia is less pronounced but failure to thrive is obvious.[ncbi.nlm.nih.gov]

  • Rieger Syndrome

    Facies: - Maxillary hypoplasia - Mild prognathism ... Teeth: - Microdontia - Hypodontia - Cone - shaped teeth ... Ear: - Abnormal ear ... Abdomen: - Umbilical hernia ...[ibis-birthdefects.org] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com]

  • Peters Anomaly

    A neonate, born to first-degree healthy cousins, presented with persistent vomiting, failure to thrive, lethargy, and jaundice.[ncbi.nlm.nih.gov] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: further delineation of the Krause-Kivlin syndrome.[emedicine.medscape.com]

  • Saethre-Chotzen Syndrome

    The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [ Figure 2 ].[ncbi.nlm.nih.gov] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] maxillary hypoplasia and relative mandibular prognathism exemplified by a prominent, wide root of the nose, thick eyebrows, prominent eyelashes, mild convergent strabismus[ncbi.nlm.nih.gov]

  • Micrognathism

    Patients are thin and show failure to thrive. Delayed motor and language development is noticed in children from an early age.[findzebra.com] […] of the teeth -Mild prognathism www.indiandentalacademy.com 19.  Hypoparathyroidism - retarded eruption -early exfoliation -enamel defects  Hyperparathyroidism - demineralization[slideshare.net] Children with micrognathia often show signs of “failure to thrive,” a term medical professionals use when children begin to fall off their growth curve.[chop.edu]

  • Familial Scaphocephaly Syndrome

    Failure to thrive can occur in the absence of nutritional support (e.g., nasogastric tube, feeding gastrostomy).[pocketdentistry.com] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] If left untreated or ineffectively treated, OSA will result in disabilities that include failure to thrive, recurrent upper respiratory infection, cognitive dysfunction, developmental[pocketdentistry.com]

  • Eyebrow Duplication - Syndactyly Syndrome

    […] to thrive Ptosis Abnormal facial shape SOURCES: MONDO UMLS OMIM ORPHANET More info about MARFAN LIPODYSTROPHY SYNDROME; MFLS Too many results?[mendelian.co] The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [Figure 2].[ijdentistry.com] […] to thrive) ( 90%) low-pitched, weak, growling cry in infancy hypertonicity (abnormally increased muscle tone) delayed bone age/skeletal abnormalities microcephaly (with possible[en.wikibooks.org]

  • Hunermann Conradi Syndrome

    […] to thrive and neurological abnormalities.[thieme-connect.com] She was determined to mandibular prognathism with mild mandibular shift to the left, maxillary deficiency, and potential involvement with a syndrome.[cyberleninka.org] All affected infants have severe failure to thrive, mental retardation, joint contractures, and cataracts.[mhmedical.com]

  • Moore-Federman Syndrome

    It is associated with failure to thrive, mental retardation, and intractable epilepsy.[mendelian.co] Physical find- ings include brachycephaly, long somewhat “coarse” face with deep skinfolds, malar and maxillary hypo- plasia, mandibular prognathism (Fig. 11, high-arched[dev.docslide.net] Thus, patients typically present in early infancy with malabsorption, steatorrhea, failure to thrive, and deficiencies of fat-soluble vitamins A, D, E, and K. [3, 4] Symptoms[emedicine.medscape.com]

  • Peters Anomaly - Cataract Syndrome

    Associated with mental retardation, hepatosplenomegaly, cirrhosis, malnutrition, and failure to thrive.[clinicalgate.com] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: further delineation of the Krause-Kivlin syndrome.[emedicine.medscape.com]

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