Infantile mercury poisoning
Synonyms: Erythroedema polyneuritis · Feer disease · Infantile acrodynia · Infantile mercury intoxication · Pink disease · Swift disease · Swift-Feer disease
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy
- Status
- active
Infantile mercury poisoning is a rare intoxication affecting children, most commonly characterized by erythema of the hands, feet and nose, edematous, painful, pink to red, desquamating fingers and toes, bluish, cold and wet extremities, excessive sweating, irritability, photophobia, muscle weakness, diffuse hypotonia, paresthesia, hypertension and tachycardia, due to elemental, organic or inorganic mercury exposure. Additional manifestations include alopecia, loss of appetite, excessive salivation with red and swollen gums, tooth and nail loss and insomnia.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infantile mercury poisoning | Erythroedema polyneuritis · Feer disease · Infantile acrodynia · Infantile mercury intoxication · Pink disease · Swift disease · Swift-Feer disease |
| fr | Intoxication infantile au mercure | Acrodynie infantile · Empoisonnement infantile au mercure · Erythroedème épidémique · Hydrargyrie infantile · Hydrargyrisme infantile · Maladie de Feer · Maladie de Swift · Maladie de Swift-Feer · Maladie rose · Polynévrite érythroedème |
| de | Quecksilbervergiftung, infantile | Feer-Krankheit · Infantile Akrodynie · Infantile Quecksilber-intoxifikation · Pink-Krankheit · Swift-Feer-Krankheit · Swift-Krankheit |
| es | Intoxicación infantil por mercurio | Acrodinia infantil · Enfermedad de Feer · Enfermedad de Pink · Enfermedad de Swift · Enfermedad de Swift-Feer · Envenenamiento infantil por mercurio |
| it | Avvelenamento infantile da mercurio | Acrodinia infantile · Eritroedema polineuritico · Intossicazione infantile da mercurio · Malattia di Feer · Malattia di Pink · Malattia di Swift · Malattia di Swift-Feer |
| nl | Infantiele kwikvergiftiging | Pink disease · Ziekte van Feer · Ziekte van Swift · Ziekte van Swift-Feer · Erytroedema polyneuritis · Infantiele acrodynie · Infantiele kwikintoxicatie |
| pt | Envenenamento da infância por mercúrio | |
| pl | Zatrucie rtęcią u dzieci | Choroba Feera · Choroba Pinka · Choroba Swifta · Choroba Swifta i Feera · Dziecięca akrodynia · Infantile mercury intoxication · Obrzęk z zaczerwienieniem z powodu zapalenia wielonerwowego |
| cs | Infantilní otrava rtutí | Erythroedema polyneuropathia · Feerova nemoc · Infantilní akrodynie · Infantilní intoxikace rtutí · Swiftova nemoc · Swiftova-Feerova nemoc · Růžová nemoc · Swift-Feerova nemoc |
| uk | Інфантильне отруєння ртуттю | Еритреїдальний поліневрит · Хвороба Фейера · Інфантильна акродинія · Дитяча ртутна інтоксикація · Рожева хвороба · Хвороба Свіфта · Хвороба Свіфта-Фейера |
| zh | 小儿铅中毒 | 小儿贡中毒 |
| tr | İnfantil cıva zehirlenmesi | Feer hastalığı · Pembe hastalık · Swift hastalığı · Swift-Feer hastalığı · İnfantil akrodinya · Eritroödem polinürit · İnfantil cıva zehirlenmesi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | T56.1 | NTBT | attributed | validated |
| ICD-11 | NE61 | NTBT | index | validated |
| MONDO | 0016588 | E | validated | |
| UMLS | C4553710 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:556508Rare disorder due to poisoning
rare disorders due to toxic effects
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/247165
- This record as JSON: /data/d/247165.json