Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Adams-Oliver syndrome (AOS) is a congenital condition marked by aplasia cutis congenita and terminal limb defects, often accompanied by diverse systemic manifestations. We present a case of a newborn female with scalp aplasia cutis and brachydactyly, but no internal organ involvement. Clinical and imaging assessments identified a scalp bone defect without neurological or cardiac abnormalities. Surgical correction of the scalp lesion was successfully performed. This case underscores the variable clinical presentation of AOS and highlights the need for comprehensive evaluation and multidisciplinary care. Early diagnosis and genetic counseling remain crucial for accurate prognosis and informed family planning.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12276772 | PMC |
http://dx.doi.org/10.7759/cureus.86442 | DOI Listing |