# Eso Pediatric Obesity Genetic Test Trigger

> This skill suggests genetic testing for pediatric patients with extreme early onset obesity (onset before 5 years of age) who exhibit clinical features of genetic obesity syndromes such as extreme hyperphagia, or who have a family history of extreme obesity. It helps clinicians identify when to refer for genetic evaluation to diagnose rare monogenic obesity syndromes.

- Skill: `dromlakhani/eso-pediatric-obesity-genetic-test-trigger` (Agent Skill)
- Install (CLI): `npx skillmds@latest add dromlakhani/eso-pediatric-obesity-genetic-test-trigger`
- Raw SKILL.md: https://api.skillmd.com/api/skills/dromlakhani/eso-pediatric-obesity-genetic-test-trigger/raw
- Safety review: pending (external: skill-scanner PASS, skillspector PASS)
- Works with: Claude Code, Claude.ai, OpenAI Codex
- Category: Coding & Dev Tools
- Author: dromlakhani (https://skillmd.com/u/dromlakhani)
- Updated: 2026-09-08
- Page: https://skillmd.com/skills/dromlakhani/eso-pediatric-obesity-genetic-test-trigger

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# Determine when to refer for genetic obesity syndrome testing

## STEP 1 — Gather Information
Record age of obesity onset, BMI percentile or % of 95th percentile, presence of extreme hyperphagia (food seeking, waking to eat), syndromic features (developmental delay, dysmorphia, hypogonadism, etc.), family history of extreme obesity, and consanguinity.

## STEP 2 — Rule In / Rule Out
If obesity onset is at or after 5 years of age, do not proceed with genetic testing for syndromic obesity; consider other etiologies such as polygenic or environmental causes.

## STEP 3 — Classify or Stratify
If extreme hyperphagia or other syndromic features are present **OR** there is a family history of extreme obesity, proceed to referral; otherwise, do not refer for genetic testing.

## STEP 4 — Decide
Order an appropriate genetic panel (e.g., leptin, leptin receptor, POMC, PCSK1, MC4R) and arrange genetic counseling for the family.

## Clinical Guardrails / Mimics / Pitfalls
Do not test patients with late-onset obesity, isolated obesity without syndromic features or family history, or those with attenuated growth suggestive of endocrine causes; avoid misattributing common polygenic obesity to monogenic syndromes and remember that Prader‑Willi syndrome typically includes developmental delay and hypotonia.

## Concrete Clinical Example
A 3‑year‑old presents with BMI 140% of the 95th percentile, incessant food‑seeking behavior, and a maternal cousin with severe early‑onset obesity; after confirming onset <5 years and extreme hyperphagia, the clinician orders leptin and leptin receptor testing and refers for genetic counseling.

**Source:** Pediatric Obesity Assessment, Treatment, and Prevention: An Endocrine Society Clinical Practice Guideline, Endocrine Society, 2017, DOI:10.1210/jc.2016-2573