TN 3 (10-99)

DI 34230.003 Multiple Body Listings from 01/06/86 to 12/11/90

110.00 MULTIPLE BODY SYSTEMS

1. A. 

   Catastrophic congenital abnormalities or disease. This section refers only to very serious congenital disorders, diagnosed in the newborn or infant child.

2. B. 

   Immune deficiency diseases. Documentation of immune deficiency disease must be submitted, and may include quantitative immunoglobulins, skin tests for delayed hypersensitivity, lymphocyte stimulative tests, and measurements of cellular immunity mediators.

110.01 CATEGORY OF IMPAIRMENTS, MULTIPLE BODY SYSTEM

110.08 Catastrophic congenital abnormalities or disease. With:

1. A. 

   A positive diagnosis (such as anencephaly, trisomy D or E, cyclopia, etc.) generally regarded as being incompatible with extra-uterine life; or

2. B. 

   A positive diagnosis (such as cri du chat, Tay-Sachs Disease) wherein attainment of the growth and development level of 2 years is not expected to occur.

110.09 Immune deficiency disease.

1. A. 

   Hypogammaglobulinemia or dysgammaglobulinimia. With:

   1. 1. 

      Recent, recurrent severe infections; or

   2. 2. 

      A complication such as growth retardation, chromic lung disease, collagen disorder, or tumors.

2. B. 

   Thymic dysplastic syndromes (such as Swiss, diGeorge).