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Amebiasis cutis
Atrophia cutis
Atrophoderma
Atrophodermia
Cutie pie
Cutie pie meter
Cutie-pie survey meter
Cutis anserina
Cutis mamelonnata
Cutis mamelonnata Pasini
Cutis marmorata
Cutis marmorata vascularis
Cutis verticis gyrata
Cutis verticis gyrata Unna-Jadassohn
Cutis verticis mamelonnata
Cutis verticis mamelonnata Pasini

Translation of "Atrophia cutis " (English → French) :

atrophoderma [ atrophodermia | atrophia cutis ]

atrophodermie
The Skin
Appareil cutané


cutie pie [ cutie-pie survey meter | cutie pie meter ]

dosimètre portatif à chambre d'ionisation
Measuring Instruments
Appareils de mesure


cutis mamelonnata | cutis mamelonnata Pasini | cutis verticis mamelonnata | cutis verticis mamelonnata Pasini

cutis mamelonnata | cutis mamelonnata de Pasini | cutis verticis mamelonnata | cutis verticis mamelonnata de Pasini
IATE - Health
IATE - Health


cutis verticis gyrata | cutis verticis gyrata Unna-Jadassohn

cutis gyrata | cutis gyrata d'Unna | cutis verticis gyrata | cutis verticis gyrata d'Unna | pachydermie plicaturée | pachydermie vorticellée du cuir chevelu
IATE - Health
IATE - Health


cutis marmorata | cutis marmorata vascularis

livedo réticulaire
IATE - Health
IATE - Health


A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax

syndrome cranio-facio-fronto-digital
SNOMEDCT-BE (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax / 763320005
SNOMEDCT-BE (disorder) / 763320005


An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterized by aplasia cutis congenita of the vertex and generalized edema (as well as hypoproteinemia and lymphopenia) due to in

aplasie cutanée congénitale autosomique récessive
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
SNOMEDCT-BE (disorder) / 720500008


An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to

syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
SNOMEDCT-BE (disorder) / 720500008


amebiasis cutis

amibiase cutanée
The Skin | Human Diseases
Appareil cutané | Maladies humaines






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'Atrophia cutis'

Date index:2023-11-20 -

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