raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:75790

Pollitt syndrome

inactive · moved to ORPHA:33364Trichothiodystrophy

Synonyms: Trichorrhexis nodosa syndrome · Trichothiodystrophy type C · Trichothiodystrophy-neurocutaneous syndrome syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Trichothiodystrophy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPollitt syndromeTrichorrhexis nodosa syndrome · Trichothiodystrophy type C · Trichothiodystrophy-neurocutaneous syndrome syndrome
frSyndrome de PollittSyndrome de trichothiodystrophie-syndrome neurocutané · Syndrome trichorrhexis nodosa
dePollitt-SyndromTrichorrhexis nodosa-Syndrom · Trichothiodystrophie - Neurokutanes Syndrom · Trichothiodystrophie Typ C
esSíndrome de PollittSíndrome de tricorrexis nodosa
itSindrome di PollittSindrome da tricoressi nodosa · Tricotiodistrofia - sindrome neurocutanea · Tricotiodistrofia, tipo C
nlSyndroom van PollittTrichorrhexis nodosa-syndroom · Trichothiodystrofie - neurocutaan syndroom-syndroom · Trichothiodystrofie type C
ptSíndrome de PollittSíndrome Tricorrexis nodosa · Tricotiodistrofia - síndrome neurocutâneo · Tricotiodistrofia tipo C
plZespół PollittaTrichotiodystrofia - zespół nerwowo-skórny · Trichotiodystrofia typu C · Zespół rozszczepu węzłowego włosa
csPollittův syndromSyndrom trichorrhexis nodosa · Trichothiodystrofie, typ C · Syndrom zahrnující trichothiodystrofii a neurokutánní syndrom
ukСиндром ПолліттаСиндром вузликового трихорексису · Трихотіодистрофія типу С · Трихотіодистрофія-нейрошкірний синдром синдром
zhPollitt综合征毛发低硫营养不良-神经皮肤综合征
trPollitt sendromuTrikotiyodistrofi tip C · Trichorrhexis nodosa sendromu · Trikotiyodistrofi-nörokutanöz sendrom sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card