raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:36236

Staphylococcal scalded skin syndrome

Synonyms: Generalized exfoliative disease · SSSS

Type
Disease
Group
Disorder
Age of onset
All ages
Status
active

A rare staphylococcal toxemia caused by epidermolytic toxins of <i>Staphylococcus aureus</i> and characterized by the appearance of widespread erythematous patches, on which large blisters develop. Upon rupture of these blisters, the skin appears reddish and scalded. The lesions typically begin in the face and rapidly expand to other parts of the body. The disease may be complicated by pneumonia and sepsis. It most commonly affects newborns and infants.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enStaphylococcal scalded skin syndromeGeneralized exfoliative disease · SSSS
frSyndrome d'épidermolyse staphylococciqueSyndrome de la peau ébouillantée · Maladie exfoliante généralisée
deStaphylococcal-Scalded-Skin-SyndromDermatitis exfoliativa neonatorum Ritter von Rittershain · SSS-Syndrom · SSSS · Staphylogene toxische epidermale Nekrolyse · Staphylogenes Lyell-Syndrom · Syndrom der verbrühten Haut
esSíndrome de la piel escaldada por estafilococosEnfermedad exfoliativa generalizada · SSSS
itSindrome cutanea combustiforme da stafilococcoMalattia esfoliativa generalizzata · SSSS
nlStaphylococcal scalded skin-syndroomGegeneraliseerde exfoliatieve ziekte · SSSS
ptDoença exfoliativa generalizada
plGronkowcowy zespół oparzeniowy skórySSSS · Uogólniona choroba złuszczająca
csStafylokokový syndrom opařené kůžeGeneralizovaná exfoliativní dermatitida · SSSS
ukСтафілококовий синдром обпеченої шкіриГенералізована ексфоліативна хвороба · SSSS
zh葡萄球菌性烫伤样皮肤综合征全身性剥脱性疾病
trStafilokokal haşlanmış deri sendromuSSSS · Jeneralize eksfolyatif hastalık

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10L00Especificvalidated
ICD-11EA50.2Especificvalidated
MONDO0018181Evalidated
MeSHD013206Evalidated
UMLSC0038165Evalidated
MedDRA10041929Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Annual incidence<1 / 1 000 0000.01 / 100 000GermanyValue and classNot yet validated15816826[PMID]
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card