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216 Possible Causes for Airway Obstruction, Round Face, Short Stature in Children

  • Mucopolysaccharidosis 2

    […] resulting in large rounded cheeks and thick lips – generally manifests between ages 18 months and four years in the early progressive form and about two years later for those[ncbi.nlm.nih.gov] Oropharyngeal and tracheobronchial deposition of glycosaminoglycans results in airway obstruction due to macroglossia, supraglottic narrowing, and tracheomalacia.[symptoma.com] The signs and symptoms may include abnormal facial features, cloudy corneas, abnormal development of spine, heart valve defects, and short stature in children A healthcare[dovemed.com]

  • Mucopolysaccharidosis

    Although upper airway obstruction was noted, it resolved with simple airway maneuvers without further airway intervention. 2017 John Wiley & Sons Ltd.[ncbi.nlm.nih.gov] Many children develop a short body trunk and a maximum stature of less than 4 feet.[en.wikipedia.org] In patients with MPS I, pre-existing upper airway obstruction may have contributed to the severity of some reactions.[biomarin.com]

  • Mucopolysaccharidosis 1

    Progressive upper airway disease leads to obstructive sleep apnoea.[patient.info] The severe form of MPS I is known as Hurler syndrome or MPS I H : Children affected with the severe form may have mental retardation, short stature, stiff joints, speech and[verywell.com] Patients present with severe airway obstructions, cranio-facial abnormalities, short neck, stiffening of the temporomandibular joints, anteriorly positioned larynx, unstable[omicsonline.org]

  • Pseudohypoparathyroidism

    obstruction.[patient.info] We report three cases of primary osteoma cutis in children, two of whom (siblings) were associated with Albright's hereditary osteodystrophy (AHO), manifesting as short stature[ncbi.nlm.nih.gov] PHP1a The constellation of PHP1a, also referred to as AHO, consists of short stature, round face, obesity, brachydactyly, brachymetacarpia, soft tissue ossification, dental[symptoma.com]

  • Prader-Willi Syndrome

    (menkes, textbook of child neurology, 5th ed, p229) Congenital neurobehavioral disorder characterized by rounded face, low forehead, almond shaped eyes, squinting, hypogonadism[icd9data.com] Descriptions of the development of symptoms of upper airway obstruction and sudden death of children with Prader-Willi Syndrome (PWS) while on GH therapy have led to concern[ncbi.nlm.nih.gov] Short stature and short hands and feet are typical of PWS. Growth retardation is common and such children fail to thrive.[symptoma.com]

  • Growth Failure

    , a temporal fat pad, round face, diabetes and other symptoms listed below.[csrf.net] Due to the limitation of smart monitor in detecting airway obstruction, clinical correlation and additional testing were recommended to rule out upper airway obstruction.[anncaserep.com] […] lead to short stature.[rileychildrens.org]

  • Achondroplasia

    face discussion; 3) edit the list and rate it in a second round.[ncbi.nlm.nih.gov] She had classical symptoms and signs of upper airway obstruction, which is often seen in patients with achondroplasia.[ncbi.nlm.nih.gov] The most common reasons for short stature in children are familial short stature, a difference in the timing of growth (called constitutional growth delay) and, in girls,[gemssforschools.org]

  • Freeman-Sheldon Syndrome

    Obstruction of the upper airway tract resulting in tracheostomy has only been described twice.[karger.com] […] forehead Intercostal myopathy Flat face Full cheeks Thickened skin over first finger Flared nostrils 2nd-5th fingers flexed towards thumb Undescended testes Contracted thumbs[syndrome.org] Freeman-Sheldon syndrome, or distal arthrogryposis type IIA (DA 2A), is a rare and severe multiple congenital contracture syndrome that is associated with upper airway obstruction[ncbi.nlm.nih.gov]

  • Vitamin D Deficiency

    NIWA provides a year round daily guide of the UV throughout New Zealand.[health.govt.nz] obstruction.[ncbi.nlm.nih.gov] However optimal vitamin D can still be produced in a few minutes if at least the face, arms and legs are exposed.[health.govt.nz]

  • Pseudohypoparathyroidism Type 1A

    In children aged 2 years, the commonest clinical features were round lunar face, obesity (70%), and subcutaneous ossifications (60%).[ncbi.nlm.nih.gov] […] on neurocognitive function in obstructive sleep apnea patients: The Apnea Positive Pressure Long-term Efficacy Study (APPLES).[karger.com] He also had congenital hypothyroidism, round face, full cheeks, shortness of limbs, mild developmental delay, and muscular hypotonia.[ncbi.nlm.nih.gov]

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