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Autosomal recessive cutis laxa type 2B
Chalazodermia
Cutis laxa
Cutis laxa senilis
Cutis laxa type
Darier-White
Dermatolysis
Hailey-Hailey
Loose skin
Pachydermatocele

Vertaling van "cutis laxa senilis " (Engels → Frans) :



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


cutis laxa | chalazodermia | dermatolysis

cutis laxa | chalazodermie | cutis hyperelastica | dermatolysie




chalazodermia | cutis laxa | dermatolysis | loose skin | pachydermatocele

chalazodermie | chalodermie | cutis hyperelastica | dermatolysie | pachydermatocèle | pachydermocèle






Abnormal palmar creases Accessory skin tags Benign familial pemphigus [Hailey-Hailey] Cutis laxa (hyperelastica) Dermatoglyphic anomalies Inherited keratosis palmaris et plantaris Keratosis follicularis [Darier-White]

Acrochordons Anomalies des dermatoglyphes Cutis laxa (hyperelastica) Kératose:folliculaire [Darier-White] | palmoplantaire héréditaire | Pemphigus bénin familial [Hailey-Hailey] Plis palmaires anormaux




Autosomal recessive cutis laxa type 2B

cutis laxa autosomique récessive type 2B




Anderen hebben gezocht naar : cutis laxa     cutis laxa senilis     darier-white     hailey-hailey     chalazodermia     cutis laxa type     dermatolysis     loose skin     pachydermatocele     


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Date index: 2024-11-22
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