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Lipodystrophy Connect is an online survey tool designed to collect demographic data and health information from individuals with Lipodystrophy.
Lipodystrophy is a heterogeneous group of rare and inherited syndromes characterized by the complete or partial loss or absence of subcutaneous adipose tissue. People living with lipodystrophy lack the fat tissue required for normal metabolic function. To enhance knowledge of the underlying biology of these conditions and to institute effective clinical treatments, the Lipodystrophy community has developed a mechanism for individuals with any of the Lipodystrophy conditions to enroll in a Lipodystrophy registry called Lipodystrophy Connect. The objective of such a registry is to create a platform that connects all of the Lipodystrophy community, including persons with Lipodystrophy, family members, healthcare providers, researchers, drug companies, advocacy groups, federal research organizations, and regulators. A patient registry will provide the foundation for a resource to meet the current and future needs of the Lipodystrophy community as well as accelerate the rate of research and development of therapies that improve the quality of life of those with Lipodystrophy. Lipodystrophy Connect is an online survey tool that collects basic demographic information and health information from people with any rare form of Lipodystrophy.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| People with Lipodystrophy & family | People currently living with lipodystrophy and their family members. |
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| Measure | Description | Time Frame |
|---|---|---|
| Descriptive epidemiology of congenital and acquired lipodystrophy. | Assessed from multiple questions regarding the natural history of patients with congenital or acquired lipodystrophy, with an emphasis on co-morbidities, history of medical evaluation or admission, and use of medications/alternative therapies. | Participants are requested to update their questionnaires every 12 months for 5 years. |
| Measure | Description | Time Frame |
|---|---|---|
| Data on disease subtype | Multiple questions about the patient's diagnostic process including reported diagnosis and subtype, time to diagnosis, method of diagnosis, age at diagnosis, presenting symptoms and specialty of diagnosing clinician. | Participants are requested to update their questionnaires every 12 months for 5 years. |
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Inclusion Criteria:
Exclusion Criteria:
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People with known or suspected lipodystrophy and their family members.
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| Name | Affiliation | Role |
|---|---|---|
| Vanessa Rangel Miller, M.S., M.B.A | PatientCrossroads | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| PatientCrossroads | San Francisco | California | 94103 | United States |
De-identified aggregate participant data is shared via a professional portal.
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| ID | Term |
|---|---|
| D008060 | Lipodystrophy |
| D052497 | Lipodystrophy, Congenital Generalized |
| D052496 | Lipodystrophy, Familial Partial |
| C562448 | Lipodystrophy, Partial, Acquired |
| ID | Term |
|---|---|
| D012875 | Skin Diseases, Metabolic |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D052439 | Lipid Metabolism Disorders |
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| Change in congenital and acquired lipodystrophy clinical features |
Assessed from multiple questions regarding the common physical features hallmark to congenital and acquired lipodystrophy. |
| Participants are requested to update their questionnaires every 12 months for 5 years. |
| Change in patient self-report Quality of Life | Assessed from self-report quality-of-life (QoL) questions about the patient's overall health, everyday living, recent impact, personal impact, available resources, diet and lifestyle history. | Participants are requested to update their questionnaires every 12 months for 5 years. |
| Data on family and reproductive history | Multiple questions regarding whether biological family members have been diagnosed with lipodystrophy or report lipodystrophy symptoms, and personal reproductive history. | Participants are requested to update their questionnaires every 12 months for 5 years. |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D008052 | Lipid Metabolism, Inborn Errors |
| D008661 | Metabolism, Inborn Errors |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D000083083 | Laminopathies |