Health Insurance (Prescribed Dental Patient) Determination 2015
I, Catherine Rule, authorised officer of the Minister for Health, make this determination under paragraph 3BA(3)(a) of the Health Insurance Act 1973.
Dated 6 July 2015
____________________________________
Catherine Rule
First Assistant Secretary
Medical Benefits Division
Department of Health
PART 1 PRELIMINARY 3
This determination is the Health Insurance (Prescribed Dental Patient) Determination 2015.
This determination commences on 6 July 2015.
The Health Insurance (Prescribed Dental Patient) Determination 2009 is
revoked.
For paragraph 3BA(3)(a) of the Health Insurance Act 1973, the definition of
a ‘prescribed dental patient’ applies to a condition specified in the Schedule
to this determination.
SCHEDULE
Specification of eligible conditions under the Cleft Lip and Cleft Palate Scheme
Conditions to which the definition of ‘prescribed dental patient’ applies: | ||
1. Oral and/or facial clefting | ||
Limited to
| Cleft lip, alveolus and/or palate | |
Tessier facial cleft | ||
2. Congenital or hereditary craniofacial malformation, deformation or disruption | ||
Limited to
| Achondroplasia | |
Branchial arch disorders including: Hemifacial/craniofacial microsomia, Goldenhar syndrome, DiGeorge syndrome, Velocardiofacial syndrome | ||
CHARGE syndrome | ||
Congenital hemifacial hyperplasia | ||
Congenital lymphatic and/or vascular malformations of the head & neck, cystic hygroma, Sturge-Weber syndrome, excluding haemangiomas, birthmarks, and naevi. | ||
Craniofacial Neurofibromatosis Type 1 | ||
Craniometaphyseal dysplasia | ||
Ectodermal dysplasia | ||
Hemifacial atrophy (Parry Romberg syndrome) | ||
Mandibulofacial dysostosis (Treacher Collins syndrome) | ||
Maxillonasal dysplasia (Binder syndrome) | ||
Oral-facial digital syndrome Type 1 | ||
Pierre Robin sequence | ||
Rubinstein-Taybi syndrome | ||
Shprintzen-Goldberg syndrome | ||
Solitary median maxillary central incisor syndrome | ||
Stickler syndrome | ||
Syndromic craniosynostoses including: Apert, Crouzon, Pfeiffer, Saethre Chotzen, and Muenke syndromes | ||
Trichorhinophalangeal syndrome Type 1 | ||
3. Hereditary conditions presenting with the absence of 6 (six) or more permanent teeth, excluding 3rd molars | ||
4. Hereditary conditions where the presence of supernumerary teeth is a major feature | ||
Limited to | Cleidocranial dysplasia | |
Gardner syndrome | ||
5. Hereditary conditions affecting the formation of enamel and/or dentine of all teeth | ||
Limited to
| Amelogenesis imperfecta | |
Dentinogenesis imperfecta | ||
Regional odontodysplasia | ||