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Retrospective analysis of the phenotypic and genotypic spectrum of mutation proven POU1F1 patients and to compare them with the published literature.

Retrospective analysis of the phenotypic and genotypic spectrum of mutation proven POU1F1 patients and to compare them with the published literature.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/05/025080
Enrollment
30
Registered
2020-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E230- Hypopituitarism

Interventions

None listed

Sponsors

Department of Endocrinology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients with growth hormone who visited the Endocrine OPD from Jan 2002 till Dec 2019.

Exclusion criteria

Exclusion criteria: 1.Mutations other than POU1F1. 2.Inadequate data 3.Insufficient Diagnosis

Design outcomes

Primary

MeasureTime frame
clinical co-relation of Genotype and Phenotype in POU1F1 Patient.Timepoint: 01 Year—

Secondary

MeasureTime frame
NoneTimepoint: 01 Year—

Countries

India

Contacts

Public ContactAnurag Ranjan Lila

KEM Hospital, Department of Endocrinology

anuraglila@gmail.com9323065346

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026