View a developmental anomaly category

Developmental anomaly categoryinformation for Malformation sequence

Description: A myelomeningocele may lead to lower limb paralysis, muscle wasting, club-foot, incontinence, renal damage, constipation and dilatation of bowel, etc. The pattern is called myelomeningocele sequence.


Developmental anomalies associated with this developmental anomaly category :

Array
(
    [Dacategory] => Array
        (
            [id] => 16
            [name] => Malformation sequence
            [description] => A myelomeningocele may lead to lower limb paralysis, muscle wasting, club-foot,  incontinence, renal damage, constipation and dilatation of bowel, etc.
The pattern is called myelomeningocele sequence.
        )

    [Thesaurus] => Array
        (
            [0] => Array
                (
                    [id] => 311
                    [name] => Cloacal dysgenesis sequence (CDS)
                    [description] => Cloacal dysgenesis sequence (CDS) is a rare cause of fetal obstructive uropathy (FOU). characteristic features are absent anal, genital, and urinary orifices associated with a smooth perineum and abnormal phallic development.
                    [author_id] => 1
                    [topo_code] => 18
                    [category_code] => 16
                    [system_code] => 6
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-30 00:00:00
                    [modified] => 2009-01-05 14:19:15
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [1] => Array
                (
                    [id] => 462
                    [name] => Prune belly syndrome
                    [description] =>  Prune belly syndrome is a group of birth abnormalities marked by three major findings:

1-Lack of development of abdominal muscles, causing the skin of the belly area to wrinkle like a prune 
2-Undescended testicles 
3-Urinary tract problems 
The amniotic fluid volume may be normal or decreased in neonates with prune belly syndrome. The presence of oligohydramnios may account for some of the accompanying findings of the extremities
 





                    [author_id] => 3
                    [topo_code] => 4
                    [category_code] => 16
                    [system_code] => 1
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 100100 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q79.4
                    [orphanet_ref] => 
                    [emedicine_ref] => eMedicine med/3055  radio/575 
                    [diseasesdb_ref] => 31089 
                    [mesh_ref] =>  D011535 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-07-24 22:26:46
                    [modified] => 2009-01-23 19:28:03
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [2] => Array
                (
                    [id] => 464
                    [name] => Myelomeningocele
                    [description] => Type of spina bifida in which the spinal cord and the meninges protrude from an opening in the spine.
                    [author_id] => 3
                    [topo_code] => 65
                    [category_code] => 16
                    [system_code] => 15
                    [parent_da_code] => 854
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q05
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-07-24 22:53:09
                    [modified] => 2009-01-05 13:40:35
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [3] => Array
                (
                    [id] => 882
                    [name] => Pierre Robin Sequence (PRS)
                    [description] => PRS is characterized by an unusually small jaw (micrognathia), posterior displacement or retraction of the tongue (glossoptosis), and upper airway obstruction. Incomplete closure of the roof of the mouth (cleft palate), is present in the majority of patients, and is commonly U-shaped.


                    [author_id] => 3
                    [topo_code] => 47
                    [category_code] => 16
                    [system_code] => 3
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 261800
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q87.0
                    [orphanet_ref] => 
                    [emedicine_ref] => ped/2680  ent/150
                    [diseasesdb_ref] => 29413
                    [mesh_ref] => D010855
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2009-01-23 19:43:17
                    [modified] => 2009-01-23 19:45:06
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

        )

)