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The head tends to be longer than normal from front to back, with a bulging forehead. This is because of the premature fusion of skull bones in the affected person.
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https://web.archive.org/web/20090106211640/http://www.mps1disease.com/patient/about/mps_pt_symptom_coarse_facial_features.asp
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Kagalwala, T. Y.; Bharucha, B. A.; Khare, R. D.; Kumta, N. B. (1 November 1988). "Diagnostic approach to coarse facies".
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Mental retardation (X-linked - epilepsy - progressive joint contractures - typical face)
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Dandy–Walker malformation (with mental retardation basal ganglia disease and seizures)
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23:) is a constellation of facial features that are present in many
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Multiple endocrine abnormalities - adenylyl cyclase dysfunction
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Several conditions are associated with coarse facial features.
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Immunodeficiency due to defect in MAPBP-interacting protein
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Mucopolysaccharidosis type 2 Hunter syndrome- severe form
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Skeletal dysplasia - coarse facies - mental retardation
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Mucopolysaccharidosis type 2 Hunter syndrome- mild form
82:"saddle-like, flat bridged nose with broad, fleshy tip"
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Mucopolysaccharidosis type I Hurler/Scheie syndrome
58:
35:
374:Spondyloepimetaphyseal dysplasia (genevieve type)
323:Neuraminidase deficiency (type II juvenile form)
364:Simpson–Golabi–Behmel syndrome - type 1 (SGBS1)
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333:Nonkeratan-sulfate-excreting Morquio syndrome
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308:Mucopolysaccharidosis type I Scheie syndrome
298:Mucopolysaccharidosis type I Hurler syndrome
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88:small, widely spaced and/or malformed teeth
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233:Mental retardation (X-linked Raynaud type)
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32:
328:Nodulosis–arthropathy–osteolysis syndrome
293:Mucopolysaccharidosis type 7 Sly syndrome
91:hypertrophic alveolar ridges and/or gums
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168:Gangliosidosis generalized GM1 (type 1)
464:. WrongDiagnosis.com. 18 November 2010
213:Infantile sialic acid storage disorder
138:Coarse face - hypotonia - constipation
7:
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318:Multiple endocrine neoplasia type 2B
188:Hyde-Forster-Mccarthy-Berry syndrome
379:Sulfatidosis juvenile (Austin type)
517:. You can help Knowledge (XXG) by
462:"Causes of Coarse facial features"
128:Börjeson–Forssman–Lehmann syndrome
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420:The Indian Journal of Pediatrics
218:Mannosidosis (alpha B lysosomal)
153:Dyggve–Melchior–Clausen syndrome
343:Sialidosis type II (congenital)
133:Chromosome 6q deletion syndrome
54:showing coarse facial features.
359:Simpson–Golabi–Behmel syndrome
348:Sialidosis type II (infantile)
1:
288:Mucopolysaccharidosis type 6
283:Mucopolysaccharidosis type 3
173:Gangliosidosis GM1 (type 3)
25:inborn errors of metabolism
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113:Alpha-mannosidosis type II
143:Congenital hypothyroidism
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338:Pituitary tumors (adult)
223:McCune–Albright syndrome
193:Hyper IgE (Job Syndrome)
253:Morquio syndrome type B
248:Morquio syndrome type A
123:Battaglia Neri syndrome
118:Aspartylglycosaminuria
17:Coarse facial features
85:large lips and tongue
79:prominent scalp veins
52:Mucopolysaccharidosis
198:Hypomelanosis of Ito
384:Winchester syndrome
238:Miescher's syndrome
163:Fucosidosis type II
76:large, bulging head
50:A 16 year old with
432:10.1007/BF02727817
178:GM1 gangliosidosis
158:Fucosidosis type 1
72:Features include:
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268:Mucolipidosis III
183:Goldberg syndrome
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30:Medical condition
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243:Morquio syndrome
65:Medical genetics
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426:(6): 861–870.
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466:. Retrieved
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558:Categories
402:References
108:Acromegaly
468:3 January
60:Specialty
448:27241573
390:See also
355:syndrome
353:Sialuria
511:symptom
440:3235137
263:MPS 3 D
258:MPS 3 C
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99:Causes
444:S2CID
515:stub
470:2011
436:PMID
428:doi
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Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
