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Translation of "monthly report " (English → French) :
TERMINOLOGY
see also In-Context Translations below 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
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
Charcot-Marie-Tooth disease, type 4F (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. It is a rare form of CMT4 but the few reported families are from diverse ethnic groups: Lebanese Shiite Muslims, Hispanic North Americans, Nor
maladie de Charcot-Marie-Tooth type 4F
SNOMEDCT-BE (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. It is a rare form of CMT4 but the few reported families are from diverse ethnic groups: Lebanese Shiite Muslims, Hispanic North Americans, Nor / 715801001
SNOMEDCT-BE (disorder) / 715801001
This syndrome is characterized by the association of global developmental delay, osteopenia and skin anomalies. To date, only three cases (two brothers and one unrelated girl) have been reported. Central nervous system anomalies manifest as poor lang
syndrome de retard de développement-ostéopénie-anomalies ectodermiques
SNOMEDCT-BE (two brothers and one unrelated girl) have been reported. Central nervous system anomalies manifest as poor lang / 717813005
SNOMEDCT-BE (disorder) / 717813005
Disease with characteristics of early-onset cerebellar signs, eye movement abnormalities and pyramidal signs. Fifty-one clinically affected members from four families (of British, Pakistani, German and French descent) have been reported to date. The
ataxie spinocérébelleuse type 11
SNOMEDCT-BE (of British, Pakistani, German and French descent) have been reported to date. The / 719207000
SNOMEDCT-BE (disorder) / 719207000
The absence or dramatic reduction of circulating human serum albumin (HSA) with less than 50 cases reported in the literature so far. In the majority of cases the disorder is diagnosed in adulthood. Although albumin is the most abundant plasma protei
analbuminémie congénitale
SNOMEDCT-BE (HSA) with less than 50 cases reported in the literature so far. In the majority of cases the disorder is diagnosed in adulthood. Although albumin is the most abundant plasma protei / 718721006
SNOMEDCT-BE (disorder) / 718721006
A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST), pulmonary chondromas and extraadrenal paragangliomas. Less than 100 cases have been reported worldwide. The disease primarily affects young women (mean age of o
triade de Carney
SNOMEDCT-BE (GIST), pulmonary chondromas and extraadrenal paragangliomas. Less than 100 cases have been reported worldwide. The disease primarily affects young women (mean age of o / 733492003
SNOMEDCT-BE (disorder) / 733492003
Pyknoachondrogenesis is a lethal skeletal osteochondrodysplasia characterised by severe generalised osteosclerosis. The disease is very rare and only five cases (four males and one female) have been reported in the literature so far. Pyknoachondrogen
pycnoachondrogénèse
SNOMEDCT-BE (four males and one female) have been reported in the literature so far. Pyknoachondrogen / 719258003
SNOMEDCT-BE (disorder) / 719258003
An extremely rare tumour association characterised by dual predisposition to melanoma and neural system tumours (typically astrocytoma). Fewer than 20 affected families have been reported to date. Affected individuals had cutaneous melanoma in associ
syndrome mélanome-tumeur du système nerveux
SNOMEDCT-BE (typically astrocytoma). Fewer than 20 affected families have been reported to date. Affected individuals had cutaneous melanoma in associ / 717968005
SNOMEDCT-BE (disorder) / 717968005
An extremely rare inborn error of sterol biosynthesis with manifestations of facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in
lathostérolose
SNOMEDCT-BE (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in / 719257008
SNOMEDCT-BE (disorder) / 719257008
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'monthly report'
Date index:2024-04-01 -
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