Fabio Pammolli, Massimo Riccaboni, Laura Magazzini, Mark Supekar

corriere

Fabio Pammolli, Massimo Riccaboni, Laura Magazzini, Mark Supekar

226

(VHL) disease

BOS syndrome Endometrial stromal sarcoma Klebsiella pneumoniae infection Paralysis periodica paramyotonica Kopysc Barczyk Krol syndrome

Boscherini Galasso Manca Bitti

Paraneoplastic cerebellar

syndrome Endomyocardial fibroelastosis Klebsiella

degeneration

Paraneoplastic Neurologic

Euhidrotic ectodermal dysplasia

Bosley-Salih-Alorainy syndrome Endomyocardial fibrosis Klebs

Disorders

Paraneoplastic neurologic

Tricho-dental syndrome

Bosma henkin christiansen syndrome Endosteal sclerosis Klebsiella infection

syndromes Tricho-dental dysplasia

Bothnian type Diffuse palmoplantar

Kleeblattschaedel-deformity Paraneoplastic pemphigus Trichodermal syndrome and mental

keratoderma Eng Strom syndrome

syndrome

(subtype)

retardation

Palmoplantar keratoderma Bothnian

Katsantoni Papadakou Lagoyanni

type Short stature locking fingers Cloverleaf skull syndrome Pemphigus

syndrome

Bothnian type Palmoplantar

Trichodermal syndrome mental

keratoderma Engelhard Yatziv syndrome Kleeblattschaedel syndrome Pemphigus vulgaris (subtype) retardation

Trichodermodysplasia dental

Bothriocephalosis Enolase deficiency type 1 Kleine-Levin syndrome Pemphigus foliaceus (subtype) alterations

Boucher Neuhauser syndrome Enolase deficiency type 2 Kleiner holmes syndrome

Hallux varus and preaxial

Paraneoplastic retinopathy Trichodysplasia

Boucher-Neuhauser syndrome Enolase deficiency type 3 polysyndactyly Cancer-associated retinopathy Trichodysplasia xeroderma

choroidal dystrophy Enolase deficiency type 4 Klinefelter's syndrome paraneurofibroma Trichoepithelioma multiple familial

Epithelioma adenoides cysticum of

Boudhina Yedes Khiari syndrome Enteric anendocrinosis

Malabsorptive diarrhea due to

Klinefelter syndrome Neurofibroma

Brooke

paucity of enteroendocrine

Paraparesis amyotrophy of hands hereditary multiple benign cystic

Bourneville syndrome

cells XXY trisomy

and feet

Epithelioma

Epithelioma hereditary multiple

Bourneville's syndrome Enterobiasis Klippel feil syndrome Parapsoriasis en plaque

benign cystic

Boutonneuse fever Human enterobiasis Fused cervical segments Parapsoriasis Tricho-hepato-enteric syndrome

Bouwes Bavinck syndrome Seatworm Klippel Feil syndrome recessive type Digitate dermatosis Tricho-hepato-enterique syndrome

Enterobius vermicularis Cervical vertebral fusion autosomal

Trichomegaly cataract hereditary

eye anomalies

infection

recessive Paraquat induced lung disease spherocytosis

Enterocyte heparan sulphate autosomal recessive Cervical

Bow leg

deficiency

vertebral fusion Paraquat poisoning Trichoodontoonychial dysplasia

Tricho-odonto-onychial dysplasia

Enterocyte intrinsic factor Klippel-feil deformity conductive Parasitic infection caused by with bone deficiency in frontoparietal

Genu varus

receptor defect of

deafness and absent vagina

Mullerian duct aplasia unilateral

Dracunculus medinensis

region

defect of Enterocyte intrinsic renal agenesis and cervicothoracic

Genu varum

factor receptor

somite anomalies

unilateral renal agenesis and

Guinea worm disease Tricho-odonto-onychial dysplasia

bowed rigid limbs and characteristic

cervicothoracic somite anomalies

Tricho-odonto-onychodysplasia with

facies Dwarfism with short Imerslund-Grasbeck syndrome Mullerian duct aplasia Guinea worm infection

syndactyly

Dwarfism with short bowed rigid Enterocyte cobalamin conductive deafness and absent

Ectodermal dysplasia with corkscrew

limbs and characteristic facies malabsorption

vagina Klippel-feil deformity

Klippel-Feil syndrome autosomal

Parastremmatic dwarfism hairs

Boomerang dysplasia Megaloblastic anemia dominant

autosomal dominant Klippel-Feil

Parastremmatic dysplasia Trueb Burg Bottani syndrome

Boomerang-like skeletal dysplasia Enteropathica

syndrome

Cervical vertebral fusion autosomal

Parathyroid carcinoma Trichophytia profunda capitis

Bowen Hutterite syndrome (formerly) Enteropathy

Enteropathy-type T-cell

dominant PARC syndrome Trichophyton infection

Bowen-Conradi Hutterite syndrome lymphoma Klippel Feil syndrome dominant type

autosomal dominant Cervical

Parchment right ventricle Kerion celsi

Bowen-Conradi syndrome Enterovirus antenatal infection vertebral fusion Parkinson disease 3 Tinea capitis profunda

BWCNS Enterovirus infection KLS PARK3

Parkinsonian features and

neurologic abnormalities mental

Susceptibility to Tinea imbricata

Envenomization by bothrops Familial hibernation (Kleine-Levin) retardation and transient psychotic

Bowenoid papulosis

lanceolatus

Envenomization by the

syndrome

episodes Trichophytia profunda barbae

Bowing congenital short bones Martinique lancehead viper

Environment associated

Familial Kleine-Levin syndrome Vitsala Tricho-retino-dento-digital syndrome

Bowing congenital with short bones hypertension Kleine-Levin hibernation syndrome Kifafa seizure disorder

mental retardation and transient

psychotic episodes Parkinsonian

features and neurologic

Trichorhinophalangeal dysplasia 1

congenital with short bones Bowing Enzyme enolase deficiency Kleine Levin Syndrome

abnormalities Giedion syndrome

Trichorhinophalangeal (TRP)

Kyphomelic dysplasia Muscle enolase deficiency Kniest like dysplasia lethal Complex familial seizure disorder syndrome 1

Bowing of long bones congenital

Bowing of the femurs aplasia or

hypoplasia of the fibula and digital

Enolase deficiency Lethal Kniest-like dysplasia Parkinsonism Trichorhinophalangeal syndrome

anomalies

aplasia or hypoplasia of the fibula

Eosinophilic cryptitis Kniest-like dysplasia Parkinson's disease TRPS

and digital anomalies Bowing of the

Trichorhinophalangeal syndrome

femurs Eosinophilic cystitis Knobloch layer syndrome Laxova-Opitz syndrome

type 1

Trichorhinophalangeal syndrome

Fuhrmann syndrome Eosinophilic enteropathy Knobloch syndrome PARKINs

type 3

Retinal detachment occipital Parkinsonism with dementia of

BPD EGE

encephalocele

Guadeloupe

Parkinsonism/Dementia complex

of Guam Amyotrophic lateral

TRPS 3

Bronchopulmonary dysplasia

Bpes without premature ovarian

Eosinophilic gastritis Knuckle pods

sclerosis Sugio-Kajii Syndrome

failure Eosinophilic gastroenteritis leuconychia Guam disease Trichoscyphodysplasia

Amyotrophic lateral sclerosis Metaphyseal chondrodysplasia with

Parkinsonism/Dementia complex cone-shaped epiphyses and

BPES type 2 Eosinophilic gastroenteropathy Kocher Debre Semelaigne disease

Association of muscular

of Guam

alopecia

pseudohypertrophy and

Amyotrophic lateral sclerosis- Metaphyseal chondrodysplasia with

Blepharophimosis syndrome type 2 Eosinophilic esophagitis hypothyroidism in children

parkinsonism/dementia complex 1 ectodermal dysplasia

Blepharophimosis ptosis and

Kocher-Debre-Semelaigne

Cupped metaphyses and cone-

epicanthus inversus type 2 Eosinophilic enteritis

syndrome Paroxysmal cold haemoglobinuria shaped epiphyses with alopecia

ptosis and epicanthus inversus type

paroxysmal familial Ventricular

2 Blepharophimosis

Blepharophimosis ptosis and

Eosinophilic fasciitis Kochs disease

fibrillation Trichothiodystrophy sun sensitivity

epicanthus inversus without

Eosinophilic lymphofollicular

Ventricular fibrillation paroxysmal

premature ovarian failure

granuloma Kohler's Disease

familial Trichothiodystrophy type B

ptosis and epicanthus inversus Eosinophilic granuloma of soft Navicular Osteochondrosis Paroxysmal ventricular fibrillation brittle hair syndrome

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