Blue sclera: Difference between revisions
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| '''Neurologic''' | | '''Neurologic''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| Bd syndrome, chitayat-moore-del bigio syndrome, daentl-townsend-siegel syndrome, developmental delay -- hypotonia extremities hypertrophy, ray-peterson-scott syndrome. | ||
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|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
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| '''Obstetric/Gynecologic''' | | '''Obstetric/Gynecologic''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Oncologic''' | | '''Oncologic''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Ophthalmologic''' | | '''Ophthalmologic''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| [[Alkaptonuria ]], Bd syndrome , Diamond-blackfan anemia]], Ehlers-danlos syndrome, Grant syndrome, [[hypophosphatasia]], [[incontinentia pigmenti ]], [[Marfan's syndrome ]], metaphyseal chondrodysplasia, recessive type, [[osteogenesis imperfecta]], [[recurrent hereditary polyserositis]], Van der hoeve's syndrome, [[Vater-like syndrome, with pulmonary hypertension, abnormal ears and growth deficiency ]]. | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Overdose / Toxicity''' | | '''Overdose / Toxicity''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Psychiatric''' | | '''Psychiatric''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| Chitayat-moore-del bigio syndrome | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Pulmonary''' | | '''Pulmonary''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Renal / Electrolyte''' | | '''Renal / Electrolyte''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| Daentl-townsend-siegel syndrome | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Rheum / Immune / Allergy''' | | '''Rheum / Immune / Allergy''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| No underlying causes | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" |
Revision as of 15:36, 20 October 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Differential Diagnosis
In alphabetical order. [1] [2]
- Alkaptonuria
- Crouzon Syndrome
- Ehlers-Danlos Syndrome
- Enlarged globe
- Infantile glaucoma
- Iron deficiency anemia
- Keratoconus
- Marfan's Syndrome
- Osteogenesis imperfecta
- Paget's Disease
- Scleral ectasia
- Scleral staphyloma
Overview
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Common Causes
Causes by Organ System
Cardiovascular | Loeys-dietz syndrome, |
Chemical / poisoning | No underlying causes |
Dermatologic | No underlying causes |
Drug Side Effect | Retigabine |
Ear Nose Throat | Van der hoeve's syndrome |
Endocrine | Laron dwarfism |
Environmental | Osteoporosis-pseudoglioma syndrome |
Gastroenterologic | No underlying causes |
Genetic | Alkaptonuria , developmental delay -- hypotonia extremities hypertrophy , ehlers-danlos syndrome , incontinentia pigmenti , juvenile paget disease, laron dwarfism, lobstein disease , loeys-dietz syndrome, marfan's syndrome , marshall-smith-weaver syndrome, metaphyseal chondrodysplasia, recessive type , osteogenesis imperfecta, paget disease juvenile type, recurrent hereditary polyserositis, willems de vries syndrome. |
Hematologic | Diamond-blackfan anemia, hypophosphatasia, |
Iatrogenic | No underlying causes |
Infectious Disease | No underlying causes |
Musculoskeletal / Ortho | Ehlers-danlos syndrome , juvenile paget disease , lobstein disease , loeys-dietz syndrome, marfan's syndrome , marshall-smith-weaver syndrome, metaphyseal chondrodysplasia, recessive type , osteogenesis imperfecta, osteoporosis-pseudoglioma syndrome , paget disease juvenile type , pelvic dysplasia arthrogryposis of lower limbs , pilo dento ungular dysplasia -- microcephaly , pseudoxanthoma elasticum, ray-peterson-scott syndrome , spondyloepimetaphyseal dysplasia joint laxity , van der hoeve's syndrome. |
Neurologic | Bd syndrome, chitayat-moore-del bigio syndrome, daentl-townsend-siegel syndrome, developmental delay -- hypotonia extremities hypertrophy, ray-peterson-scott syndrome. |
Nutritional / Metabolic | Alkaptonuria , hypophosphatasia. |
Obstetric/Gynecologic | No underlying causes |
Oncologic | No underlying causes |
Ophthalmologic | Alkaptonuria , Bd syndrome , Diamond-blackfan anemia]], Ehlers-danlos syndrome, Grant syndrome, hypophosphatasia, incontinentia pigmenti , Marfan's syndrome , metaphyseal chondrodysplasia, recessive type, osteogenesis imperfecta, recurrent hereditary polyserositis, Van der hoeve's syndrome, Vater-like syndrome, with pulmonary hypertension, abnormal ears and growth deficiency . |
Overdose / Toxicity | No underlying causes |
Psychiatric | Chitayat-moore-del bigio syndrome |
Pulmonary | No underlying causes |
Renal / Electrolyte | Daentl-townsend-siegel syndrome |
Rheum / Immune / Allergy | No underlying causes |
Sexual | No underlying causes |
Trauma | No underlying causes |
Urologic | No underlying causes |
Miscellaneous | Foreign body |