Protocol - Family History of Speech and Language Impairment
- Early Childhood Speech and Language Assessment - Ages and Stages Questionnaire
- Early Childhood Speech and Language Assessment - Speech and Language Assessment Scale
- Family History of Speech and Language Impairment
- Grammatical Impairments - Clinical Evaluation of Language Fundamentals
- Grammatical Impairments - Grammaticality Judgment Task
- Grammatical Impairments - Test of Early Grammatical Impairment
Description
The Family History Questionnaire is a 9-item proxy-administered questionnaire completed by a parent for their young child. It asks about the child's personal and family history of speech and language impairment.
Specific Instructions
Rosa's Law, enacted in October 2010, changes references in federal laws and acts from "mental retardation" to "intellectual disability," and references to a "mentally retarded individual" to "an individual with an intellectual disability." The PhenX Working Group notes that this protocol was developed and tested using previously accepted terminology. Replacing this terminology with the newly enacted standard is at the researcher's discretion.
The Expert Review Panel recommends that items 11 through 21 (hereditary factors) of the Personal and Family History of Hearing Loss protocol are added to this protocol.
Availability
Protocol
Family History Questionnaire
Target child/person items:
1. By age 2, was your child talking in short phrases or sentences?
0[ ]No
1[ ]Yes
99[ ]Don't Know
2. When your child was 2 years old, were you concerned that he/she was having difficulty learning to talk?
0[ ]No
1[ ]Yes
99[ ]Don't Know
3. At this time, do people frequently have trouble understanding your child?
0[ ]No
1[ ]Yes
99[ ]Don't Know
4. Has anyone in your child's family had speech or language therapy?
0[ ]No
1[ ]Yes
99[ ]Don't Know
If Yes, Relationship to child? ___________________________________
What for? ____________________________________
Family items
Family: Parents and biologically related siblings
5. Has anyone in your child's family had difficulty learning to read or had problems with school work? (e.g., repeated a grade)
0[ ]No
1[ ]Yes
99[ ]Don't Know
If Yes, what are the details? _________________________________________
6. Has anyone in your child's family been diagnosed as mentally retarded?
0[ ]No
1[ ]Yes
99[ ]Don't Know
7. Does anyone in your child's family have a hearing difficulty?
0[ ]No
1[ ]Yes
99[ ]Don't Know
8. Has anyone in your child's family been slow in learning to talk?
0[ ]No
1[ ]Yes
99[ ]Don't Know
9. Has anyone in your child's family had any other type of communication disorder such as:
9.1. Stuttering?
0[ ]No
1[ ]Yes
9.2. Is less talkative?
0[ ]No
1[ ]Yes
9.3. Has a hard time carrying on a conversation?
0[ ]No
1[ ]Yes
9.4. Doesn't like to read?
0[ ]No
1[ ]Yes
9.5. Doesn't read well?
0[ ]No
1[ ]Yes
9.6. Has difficulty thinking of words (s)he wants to say when talking?
0[ ]No
1[ ]Yes
9.7. Has a poorer vocabulary than other family members?
0[ ]No
1[ ]Yes
9.8. Is a poor speller?
0[ ]No
1[ ]Yes
9.9. Has awkward sentence structures when writing or talking?
0[ ]No
1[ ]Yes
9.10. Mispronounces long words?
0[ ]No
1[ ]Yes
9.11. Is hard to follow when (s)he tells you something, such as a personal experience?
0[ ]No
1[ ]Yes
9.12. Has difficulty explaining things?
0[ ]No
1[ ]Yes
Personnel and Training Required
None
Equipment Needs
The respondent will need a copy of the questionnaire.
Requirements
Requirement Category | Required |
---|---|
Major equipment | No |
Specialized training | No |
Specialized requirements for biospecimen collection | No |
Average time of greater than 15 minutes in an unaffected individual | No |
Mode of Administration
Proxy-administered questionnaire
Lifestage
Child, Adolescent, Adult
Participants
The parents of children and adolescents, ages 3-21 years old
Selection Rationale
The Family History Questionnaire was selected because it is a simple, reliable protocol that can be quickly and easily administered to capture a child's personal and family history of speech and language impairment.
Language
Chinese, English
Standards
Standard | Name | ID | Source |
---|---|---|---|
Logical Observation Identifiers Names and Codes (LOINC) | Fam hx speech lang impair proto | 62984-0 | LOINC |
Human Phenotype Ontology | Poor speech | HP:0002465 | HPO |
Human Phenotype Ontology | Delayed speech and language development | HP:0000750 | HPO |
Human Phenotype Ontology | Speech articulation difficulties | HP:0009088 | HPO |
Human Phenotype Ontology | Incomprehensible speech | HP:0002546 | HPO |
Human Phenotype Ontology | Slurred speech | HP:0001350 | HPO |
Human Phenotype Ontology | Dysarthria | HP:0001260 | HPO |
caDSR Form | PhenX PX200401 - Family History Of Speech And Language Impairment | 6196033 | caDSR Form |
Derived Variables
None
Process and Review
The Expert Review Panel #7 (ERP 7) reviewed the measures in the Speech and Hearing domain.
Guidance from ERP 7 includes the following:
- Minor changes to specific instructions
Protocol Name from Source
Family History Questionnaire
Source
Mabel L. Rice, author. Family History Questionnaire. Language Acquisition Studies Lab. University of Kansas, Lawrence, KS.
General References
Rice, M. L., Haney, K. R., & Wexler, K. (1998). Family histories of children with SLI who show extended optional infinitives. Journal of Speech, Language, and Hearing Research, 41, 419–432.
Protocol ID
200401
Variables
Export VariablesVariable Name | Variable ID | Variable Description | dbGaP Mapping | |
---|---|---|---|---|
PX200401_Family_History_Speech_Language_Impairment_Awkward_Sentence_Structure | ||||
PX200401090900 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Difficulty_Explaining_Things | ||||
PX200401091200 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Difficulty_Learning_Read | ||||
PX200401050100 | Has anyone in your child's family had more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Difficulty_Learning_Read | ||||
PX200401050000 | Has anyone in your child's family had more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Difficulty_Learning_Talk | ||||
PX200401020000 | When your child was two years old, were you more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Does_Not_Read | ||||
PX200401090400 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Does_Not_Read_Well | ||||
PX200401090500 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Hard_Follow | ||||
PX200401091100 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Hearing_Difficulty | ||||
PX200401070000 | Does anyone in your child's family have a more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Less_Talkative | ||||
PX200401090200 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Mispronounce_Long_Words | ||||
PX200401091000 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Poorer_Vocabulary | ||||
PX200401090700 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Poor_Speller | ||||
PX200401090800 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Retardation | ||||
PX200401060000 | Has anyone in your child's family been more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Slow_Talk | ||||
PX200401080000 | Has anyone in your child's family been slow more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Speech_Language_Therapy | ||||
PX200401040100 | Has anyone in your child's family had speech more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Speech_Language_Therapy | ||||
PX200401040000 | Has anyone in your child's family had speech more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Speech_Language_Therapy_Relationship | ||||
PX200401040200 | Has anyone in your child's family had speech more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Stuttering | ||||
PX200401090100 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Talking_Short_Sentences | ||||
PX200401010000 | By age 2, was your child talking in short more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Thinking_Words | ||||
PX200401090600 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Trouble_CarryOn_Conversation | ||||
PX200401090300 | Has anyone in your child's family had any more | N/A | ||
PX200401_Family_History_Speech_Language_Impairment_Trouble_Understanding_Child | ||||
PX200401030000 | At this time, do people frequently have more | N/A |
Measure Name
Family History of Speech and Language Impairment
Release Date
October 8, 2010
Definition
This measure is a questionnaire to identify family history of speech and language impairment.
Purpose
This measure can be used to assess familial risk factors related to speech and language impairment.
Keywords
Family History, Speech, language, speech and hearing
Measure Protocols
Protocol ID | Protocol Name |
---|---|
200401 | Family History of Speech and Language Impairment |
Publications
Andres, E. M., et al. (2021) Study of rare genetic variants in TM4SF20, NFXL1, CNTNAP2, and ATP2C2 in Pakistani probands and families with language impairment. Meta Gene. 2021 December; 30: 100966. doi: 10.1016/j.mgene.2021.100966
Andres, E. M., et al. (2019) A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI)." . European Journal of Human Genetics. 2019 April; 27(8): 1274-1285. doi: 10.1038/s41431-019-0398-1
Rice, M.L. & Tager-Flusberg, H. (2016) Language Phenotypes. In V. Jagaroo and S.L. Santangelo (eds.) Neurophenotypes, Innovations in Cognitive Neuroscience. Springer. 2016 January; doi: 10.1007/978-1-4614-3846-5_12