Bill Text: TX HB2295 | 2025-2026 | 89th Legislature | Introduced


Bill Title: Relating to newborn screening tests for Duchenne muscular dystrophy.

Spectrum: Partisan Bill (Republican 2-0)

Status: (Introduced) 2025-01-30 - Filed [HB2295 Detail]

Download: Texas-2025-HB2295-Introduced.html
  89R9499 EAS-F
 
  By: Capriglione H.B. No. 2295
 
 
 
A BILL TO BE ENTITLED
 
AN ACT
  relating to newborn screening tests for Duchenne muscular
  dystrophy.
         BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:
         SECTION 1.  The heading to Chapter 33, Health and Safety
  Code, is amended to read as follows:
  CHAPTER 33. DUCHENNE MUSCULAR DYSTROPHY, PHENYLKETONURIA, OTHER
  HERITABLE DISEASES, HYPOTHYROIDISM, AND CERTAIN OTHER DISORDERS
         SECTION 2.  Section 33.001, Health and Safety Code, is
  amended by adding Subdivision (6) to read as follows:
               (6)  "Duchenne muscular dystrophy" means a progressive
  muscular degeneration disorder caused by alterations of the protein
  dystrophin and characterized by progressive muscle degeneration
  and weakness.
         SECTION 3.  Sections 33.002(a) and (c), Health and Safety
  Code, are amended to read as follows:
         (a)  The department shall carry out a program to combat
  morbidity, including intellectual disability, and mortality in
  persons who have Duchenne muscular dystrophy, phenylketonuria,
  other heritable diseases, or hypothyroidism.
         (c)  The department shall establish and maintain a
  laboratory to:
               (1)  conduct experiments, projects, and other
  activities necessary to develop screening or diagnostic tests for
  the early detection of Duchenne muscular dystrophy,
  phenylketonuria, other heritable diseases, and hypothyroidism;
               (2)  develop ways and means or discover methods to be
  used to prevent or treat Duchenne muscular dystrophy,
  phenylketonuria, other heritable diseases, and hypothyroidism; and
               (3)  serve other purposes considered necessary by the
  department to carry out the program.
         SECTION 4.  Section 33.011(a), Health and Safety Code, is
  amended to read as follows:
         (a)  The physician attending a newborn child or the person
  attending the delivery of a newborn child that is not attended by a
  physician shall cause the child to be subjected to screening tests
  approved by the department for Duchenne muscular dystrophy,
  phenylketonuria, other heritable diseases, hypothyroidism, and
  other disorders for which screening is required by the department.
         SECTION 5.  Section 33.014(a), Health and Safety Code, is
  amended to read as follows:
         (a)  If, because of an analysis of a specimen submitted under
  Section 33.011, the department reasonably suspects that a newborn
  child may have Duchenne muscular dystrophy, phenylketonuria,
  another heritable disease, hypothyroidism, or another disorder for
  which the screening tests are required, the department shall notify
  the person who submits the specimen that the results are abnormal
  and provide the test results to that person. The department may
  notify one or more of the following that the results of the analysis
  are abnormal and recommend further testing when necessary:
               (1)  the physician attending the newborn child or the
  physician's designee;
               (2)  the person attending the delivery of the newborn
  child that was not attended by a physician;
               (3)  the parents of the newborn child;
               (4)  the health authority of the jurisdiction in which
  the newborn child was born or in which the child resides, if known;
  or
               (5)  physicians who are cooperating pediatric
  specialists for the program.
         SECTION 6.  Section 33.031(a), Health and Safety Code, is
  amended to read as follows:
         (a)  All newborn children and other individuals under 21
  years of age who have been screened, have been found to be
  presumptively positive through the newborn screening program for
  Duchenne muscular dystrophy, phenylketonuria, other heritable
  diseases, hypothyroidism, or another disorder for which the
  screening tests are required, and may be financially eligible may
  be referred to the department's services program for children with
  special health care needs.
         SECTION 7.  Section 33.032(a), Health and Safety Code, is
  amended to read as follows:
         (a)  Within the limits of funds available for this purpose
  and in cooperation with the individual's physician, the department
  may provide services directly or through approved providers to
  individuals of any age who meet the eligibility criteria specified
  by department rules on the confirmation of a positive test for
  Duchenne muscular dystrophy, phenylketonuria, other heritable
  diseases, hypothyroidism, or another disorder for which the
  screening tests are required.
         SECTION 8.  Section 203.355(c), Occupations Code, is amended
  to read as follows:
         (c)  The laboratory services must include the performance of
  the standard serological tests for syphilis and the collection of
  blood specimens for newborn screening tests for Duchenne muscular
  dystrophy, phenylketonuria, hypothyroidism, and other heritable
  diseases as required by law.
         SECTION 9.  Not later than September 1, 2027, the Department
  of State Health Services shall implement the changes in law made by
  this Act to the newborn screening program under Chapter 33, Health
  and Safety Code.
         SECTION 10.  This Act takes effect September 1, 2025.
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