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reduced results from
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18B options
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960000
reduced results due to: symptoms, possible diagnoses, age, gender
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128000
reduced results due to: duration, diagnostic tests, modifiers
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4
options
reduced results due to: first pass, final pass
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refinement options
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duration of symptoms:
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lifestyle modifiers
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family history of
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1 - 4 of 4 diseases -
gender ?
age ?
strange cry
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score graph
The score graph represents the results on the x axis and the "score" on the y axis. The purpose of this graph is to visually display the relative scores and how dramatically or not the likelihood of the diseases compare.
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Show only results from category
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weighted category breakdown
This pie chart represents the results broken down categorically. The size of the pie, or "score" of the category, is the sum of the scores of the diseases in the category. Please note a disease may fall into multiple category.
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|muscle weakness in foot (feet)|limited neck movements|impaired sensations in foot (feet)|delayed development|LIFESTYLE - Family History|DEMOGRAPHIC - age|DEMOGRAPHIC - duration|)
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variable sensitivity
This bar chart represents the variables that the results and their ordering are most sensitive too.
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The results should NOT be considered a diagnosis.
Please consult your health care provider.
edit important variables such as:
demo: duration, demo: age, life: Family History, delayed development, impaired sensations in foot (feet), limited neck movements, muscle weakness in foot (feet)
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Basilar impression - congenital abnormality at junction of head and neck
a.k.a Bull-Nixon syndrome
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Dubowitz Syndrome - rare genetic disorder with small head and typical facial appearance
a.k.a intrauterine dwarfism, Prader-willi syndrome
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Dubowitz Syndrome
genetic or congenital
[chronic]
face deformities, peeling of skin, scaly patches on skin, short attention span
Dubowitz syndrome is a rare genetic disorder characterized by microcephaly, growth retardation and a characteristic facial appearance (small, round, triangular shaped with a pointed, receding chin, a broad, wide-tipped nose, and wide-set eyes with drooping eyelids.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Weaver Syndrome - rare congenital disorder with rapid growth
a.k.a Weaver-Williams syndrome
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Cri-du-chat Syndrome - syndrome that occurs from missing a piece of chromosome 5
a.k.a cri-du-chat syndrome, chromosome 5p deletion syndrome, 5p minus syndrome, Lejeune’s syndrome
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Known synonyms for your symptoms:
• abnormal cry -
strange cry , cry abnormal , cry strange , cry weird ,
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