25 Tex. Admin. Code § 37.52
Definitions
Effective Aug 1, 200429 TexReg 7101Source Note: The provisions of this §37.52 adopted to be effective February 2, 1989, 13 TexReg 6268; amended to be effective May 16, 1994, 19 TexReg 3369; amended to be effective December 17, 2002, 27 TexReg 11744; amended to be effective August 1, 2004, 29 TexReg 7101.Texas Secretary of State
The following words and terms, when used in these sections, shall have the following meanings, unless the context clearly indicates otherwise.
- (1) Board--The Texas Board of Health or its successor.
(2) Bona fide resident--A person who:
- (A) is physically present within the geographic boundaries of the state;
- (B) has an intent to remain within the state;
- (C) maintains an abode within the state (i.e., house or apartment, not merely a post office box);
- (D) has not come to Texas from another country for the purpose of obtaining medical care, with the intent to return to the person's native country;
(E) does not claim residency in any other state or country; and
- (i) is a minor child residing in Texas whose parent(s), managing conservator, or guardian of the child's person is a bona fide resident;
- (ii) is a person residing in Texas who is the legally dependent spouse of a bona fide resident; or
- (iii) is an adult residing in Texas, including an adult whose legal guardian is a bona fide resident or who is his/her own guardian.
- (3) Commissioner--The commissioner of health or his successor.
- (4) Congenital adrenal hyperplasia--An inherited condition which may lead to serious illness and death if not treated.
- (5) Department--The Texas Department of Health or its successor.
- (6) Galactose-1-phosphate uridyltransferase deficiency--An inherited condition, which if not treated, may cause fatal infection or mental retardation.
- (7) Homocystinuria--An inherited condition, which if not treated, may cause mental retardation, blood clots, vision problems, skeletal abnormalities, and possibly death.
- (8) Hypothyroidism--A condition which, if not treated, leads to mental and physical retardation.
- (9) Phenylketonuria or PKU--An inherited condition, which if not treated may cause severe mental retardation.
- (10) Program--The Newborn Screening Program of the department.
- (11) Program administrator--The individual employed by the department who administrates and or manages the follow-up portion of the program.
- (12) Satisfactory specimen--A blood specimen obtained by uniform absorption onto a filter paper target such that complete filling of the target is realized through to both front and back of the paper.
- (13) Screening test, screen, or test--A test or battery of tests for the rapid determination of the need for a medical evaluation.
- (14) Services--Those benefits identified by the board in §37.60 of this title (relating to Scope of Newborn Screening Program Services).
- (15) Sickling hemoglobinopathy (including sickle cell disease)--An inherited condition, which predisposes an individual to fatal infection and interrupted blood supply to vital organs.
Source Note:The provisions of this §37.52 adopted to be effective February 2, 1989, 13 TexReg 6268; amended to be effective May 16, 1994, 19 TexReg 3369; amended to be effective December 17, 2002, 27 TexReg 11744; amended to be effective August 1, 2004, 29 TexReg 7101.