Seckel syndrome: Difference between revisions
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'''Seckel syndrome 1''': Bird-headed dwarfism; Microcephalic Primordial Dwarfism 1; Nanocephalic dwarfism; Seckel-type dwarfism | '''Seckel syndrome 1''': Bird-headed dwarfism; Microcephalic Primordial Dwarfism 1; Nanocephalic dwarfism; Seckel-type dwarfism | ||
'''Seckel syndrome 2''': Bird-headed dwarfism 2; Microcephalic Primordial Dwarfism 2; Seckel-type dwarfism 2 | '''Seckel syndrome 2''': Bird-headed dwarfism 2; Microcephalic Primordial Dwarfism 2; Seckel-type dwarfism 2 |
Revision as of 15:19, 19 November 2013
WikiDoc Resources for Seckel syndrome |
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Most recent articles on Seckel syndrome Most cited articles on Seckel syndrome |
Media |
Powerpoint slides on Seckel syndrome |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Seckel syndrome at Clinical Trials.gov Trial results on Seckel syndrome Clinical Trials on Seckel syndrome at Google
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US National Guidelines Clearinghouse on Seckel syndrome NICE Guidance on Seckel syndrome
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Seckel syndrome Discussion groups on Seckel syndrome Patient Handouts on Seckel syndrome Directions to Hospitals Treating Seckel syndrome Risk calculators and risk factors for Seckel syndrome
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Causes & Risk Factors for Seckel syndrome |
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Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vidit Bhargava, M.B.B.S [2]
Synonyms and keywords:
Seckel syndrome 1: Bird-headed dwarfism; Microcephalic Primordial Dwarfism 1; Nanocephalic dwarfism; Seckel-type dwarfism Seckel syndrome 2: Bird-headed dwarfism 2; Microcephalic Primordial Dwarfism 2; Seckel-type dwarfism 2
Overview
The Seckel syndrome or microcephalic primordial dwarfism is a congenital nanosomic disorder supposed to be caused by defects of genes onchromosome 3 and 18. One form of Seckel syndrome can be caused by mutation in the gene encoding ataxia-telangiectasia and RAD3-related protein (ATR) which maps to chromosome 3q22.1-q24. This gene is central in the cell's DNA damage response and repair mechanism.
Historical Perspective
Classification
Pathophysiology
Genetics
Associated Conditions
Gross Pathology
Microscopic Pathology
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 | No underlying causes |
Chemical / poisoning | No underlying causes |
Dermatologic | No underlying causes |
Drug Side Effect | No underlying causes |
Ear Nose Throat | No underlying causes |
Endocrine | No underlying causes |
Environmental | No underlying causes |
Gastroenterologic | No underlying causes |
Genetic | No underlying causes |
Hematologic | No underlying causes |
Iatrogenic | No underlying causes |
Infectious Disease | No underlying causes |
Musculoskeletal / Ortho | No underlying causes |
Neurologic | No underlying causes |
Nutritional / Metabolic | No underlying causes |
Obstetric/Gynecologic | No underlying causes |
Oncologic | No underlying causes |
Opthalmologic | No underlying causes |
Overdose / Toxicity | No underlying causes |
Psychiatric | No underlying causes |
Pulmonary | No underlying causes |
Renal / Electrolyte | No underlying causes |
Rheum / Immune / Allergy | No underlying causes |
Sexual | No underlying causes |
Trauma | No underlying causes |
Urologic | No underlying causes |
Dental | No underlying causes |
Miscellaneous | No underlying causes |
Causes in Alphabetical Order
- A...
- Z...
Make sure that each diagnosis is linked to a page.
Differentiating type page name here from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History
A directed history should be obtained to ascertain
Symptoms
- Achondroplasia
- Cryptorchidism
- Dislocations of pelvis and elbow
- Low birth weight
- Low ears
- Microcephaly
- Pancytopenia
- Severe mental retardation (more than half of the patients have an IQ below 50)
- Small chin
- Unusually large eyes