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358 Possible Causes for High Arched Palate, Marfan Syndrome, Speech Delay

  • Homocystinuria

    Early signs of myopia and lens abnormalities cannot be ignored. [8] Bony abnormalities and body habitus can be confused with Marfan syndrome; however, Marfan syndrome follows[] On preanesthetic check up, history revealed full term normal vaginal delivery of child and with no perinatal complications with history of speech delay at age of 3 years.[] Long, thin fingers, tall stature, and a high arched palate are seen in some individuals and the hair is often lightly pigmented.[]

  • Goldberg-Shprintzen Syndrome

    Intellectual disability is more likely to occur in those with Shprintzen-Goldberg syndrome, while heart problems are more likely to occur in Marfan syndrome.[] Medical therapies can help manage developmental delays in children with VCFS.[] […] syndrome exhibit ocular (ptosis, hyperopia, or megalocornea), cardiac, urogenital (vesicoureteral reflux, multicystic renal dysplasia), and skeletal (oligodontia, scoliosis, high-arched[]

  • Turner Syndrome

    […] and Loeys-Dietz syndromes. 28 Additional management principles used in Marfan syndrome include exercise restriction, frequent cardiovascular imaging, and prophylactic surgical[] Evaluate the child’s speech and refer the child to a speech therapist when appropriate. Consider hearing loss as a possible cause of speech delay.[] Serous otitis media is more common, probably because of low anatomic drainage of the middle ear, that may be because of high-arched palate.[]

  • Sotos Syndrome

    Two of these conditions are Marfan syndrome and Sotos syndrome.[] Our findings provide evidence for the existence of a novel syndrome of short stature, microcephaly, delayed bone development, speech delay and mild or absent facial dysmorphism[] Dental abnormalities include enamel hypoplasia, expansion of the pulp cavity, high arched palate, and absence of the bilateral pre-molar teeth of the mandible.[]

  • Rubinstein-Taybi Syndrome

    Childhood More information GENETIC TESTING AND MARFAN SYNDROME GENETIC TESTING AND MARFAN SYNDROME Genetic testing for mutations in fibrillin-1 (FBN1) and other genes has[] […] of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired speech and language development Impaired[] (RTS) is a rare disorder affecting 1 of 300,000 people, characterized by growth, mental and motor retardation, small stature, broad thumbs and toes, characteristic face, high-arched[]

  • Down Syndrome

    KF Peters, F Kong, M Hanslo and BB Biesecker , Living with Marfan syndrome III.[] There can be language development delay both from hearing impairment and speech delay.[] Mouth: Protruding tongue (small narrow palate). High arched palate. Neck: Loose skin on nape of neck. Hands: Single palmar crease. Short little finger.[]

  • Dubowitz Syndrome

    ): Beckwith-Wiedemann syndrome Sotos syndrome Weaver syndrome Q87.4 Marfan's syndrome Q87.40 Marfan's syndrome, unspecified Q87.41 Marfan's syndrome with cardiovascular manifestations[] Speech delays, an unusually soft, high-pitched voice, submucous cleft palate, and velopharyngeal insufficiency were noted in childhood.[] The mouth can have a high arched palate , submucous cleft palate , or velopharyngeal insufficiency.[]

  • Tel Hashomer Camptodactyly Syndrome

    DW (l99l) Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. ‎[] speech and language development Seizures Breast hypoplasia Nemaline bodies Eunuchoid habitus Decreased testosterone in males Type 1 muscle fiber predominance Multiple prenatal[] Features compatible with skeletal muscle and/ or connective tissue involvement include high-arched palate, hypoplastic and hypotonic muscles, scapulae ala-tae, thoracic scoliosis[]

  • MASS Syndrome

    الصفحة 33 - Pyeritz RE: Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan's syndrome. N Engl J Med 1994;330: 1335-1341. ‏[] In affected males, the onset of speech is delayed (Winter et al., 1989).[] […] this condition (OMIM #208050) are as follows: Marked tortuosity of the aorta and its branches Predisposition to aortic dissection Telangiectasias on the cheeks Lax skin High-arched[]

  • Hyperextensible Joints

    Aortic Dissection Hypermobile Joints Marfan Syndrome Ehlers Danlos Hypermobility Rn School Chiari Malformation Flat Feet Body Systems Scoliosis Forward Marfan Syndrome Symptoms[] delay seizures Physical features associated with fragile X syndrome can be subtle and difficult to identify and diagnose accurately, especially in younger children.[] arched palate[ 25 ].[]

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