Aplasia cutis congenita-intestinal lymphangiectasia syndrome | |
---|---|
Specialty | Medical genetics |
Symptoms | A combination of aplasia cutis congenita and lymphangiectasia |
Complications | Death |
Usual onset | Birth |
Prevention | none |
Prognosis | Bad |
Frequency | very rare, only two cases have been described in medical literature |
Deaths | - |
Aplasia cutis congenita-intestinal lymphangiectasia syndrome is a very rare genetic disorder which is characterized by aplasia cutis congenita, intestinal lymphangiectasia-induced generalized edema, hypoproteinemia, and lymphopenia. [1] [2] It has been described in two Ashkenazi Jewish brothers. [3] [4]
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cite web}}
: CS1 maint: numeric names: authors list (
link)
Aplasia cutis congenita-intestinal lymphangiectasia syndrome | |
---|---|
Specialty | Medical genetics |
Symptoms | A combination of aplasia cutis congenita and lymphangiectasia |
Complications | Death |
Usual onset | Birth |
Prevention | none |
Prognosis | Bad |
Frequency | very rare, only two cases have been described in medical literature |
Deaths | - |
Aplasia cutis congenita-intestinal lymphangiectasia syndrome is a very rare genetic disorder which is characterized by aplasia cutis congenita, intestinal lymphangiectasia-induced generalized edema, hypoproteinemia, and lymphopenia. [1] [2] It has been described in two Ashkenazi Jewish brothers. [3] [4]
{{
cite web}}
: CS1 maint: numeric names: authors list (
link)