Breast carcinoma, and Finger syndactyly

Diseases related with Breast carcinoma and Finger syndactyly

In the following list you will find some of the most common rare diseases related to Breast carcinoma and Finger syndactyly that can help you solving undiagnosed cases.


Top matches:

Medium match SAETHRE-CHOTZEN SYNDROME


Saethre-Chotzen syndrome (SCS) is an inherited craniosynostosis syndrome characterized by unilateral or bilateral coronal synostosis, facial asymmetry, ptosis, strabismus and small ears with prominent crus, among other less common manifestations.

SAETHRE-CHOTZEN SYNDROME Is also known as acs3|acrocephalosyndactyly type 3|scs|acrocephaly, skull asymmetry, and mild syndactyly|acs iii|acrocephalosyndactyly, type iii|chotzen syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about SAETHRE-CHOTZEN SYNDROME

Low match ADULT SYNDROME


ADULT (Acro-dermo-ungual-lacrimal-tooth) syndrome is a rare ectodermal dysplasia syndrome (see this term) characterized by ectrodactyly, syndactyly, mammary hypoplasia, and excessive freckling as well as other typical ectodermal defects such as hypodontia, lacrimal duct anomalies, hypotrichosis, and onychodysplasia.

ADULT SYNDROME Is also known as acrodermatounguallacrimaltooth syndrome|pigment anomaly-ectrodactyly-hypodontia syndrome|acro-dermato-ungual-lacrimal-tooth syndrome

Related symptoms:

  • Brachydactyly
  • Wide nasal bridge
  • Abnormality of the dentition
  • Syndactyly
  • Midface retrusion


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about ADULT SYNDROME

Low match APOCRINE GLAND SECRETION, VARIATION IN


APOCRINE GLAND SECRETION, VARIATION IN Is also known as cerumen, variation in|wet wax|ww|colostrum secretion, variation in|ear wax, wet/dry|axillary odor, variation in|ewwd

Related symptoms:

  • Neoplasm
  • Breast carcinoma
  • Abnormality of the ear


SOURCES: OMIM MENDELIAN

More info about APOCRINE GLAND SECRETION, VARIATION IN

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Other less relevant matches:

Low match LIMB-MAMMARY SYNDROME


Limb-mammary syndrome (LMS) is a rare disease belonging to the group of ectodermal dysplasias.

LIMB-MAMMARY SYNDROME Is also known as lms

Related symptoms:

  • Cleft palate
  • Syndactyly
  • Hypogonadism
  • Camptodactyly
  • Hypodontia


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about LIMB-MAMMARY SYNDROME

Low match ZLOTOGORA-OGUR SYNDROME


Zlotogora-Ogur syndrome is an ectodermal dysplasia syndrome characterized by hair, skin and teeth anomalies, facial dysmophism with cleft lip and palate, cutaneous syndactyly and, in some cases, intellectual disability.

ZLOTOGORA-OGUR SYNDROME Is also known as cleft lip/palate-ectodermal dysplasia syndrome|clped1|ed4|syndactyly-ectodermal dysplasia-cleft/lip palate|cleft lip/palate-syndactyly-pili torti syndrome|ectodermal dysplasia, margarita island type|ectodermal dysplasia, cleft lip and palate, mental retar

Related symptoms:

  • Intellectual disability
  • Seizures
  • Micrognathia
  • Cleft palate
  • Wide nasal bridge


SOURCES: ORPHANET OMIM MENDELIAN

More info about ZLOTOGORA-OGUR SYNDROME

Low match ROSSELLI-GULIENETTI SYNDROME


Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Micrognathia
  • Cleft palate


SOURCES: OMIM MENDELIAN

More info about ROSSELLI-GULIENETTI SYNDROME

Low match FRASER SYNDROME


Fraser syndrome is a rare clinical entity including as main characteristics cryptophthalmos and syndactyly.

FRASER SYNDROME Is also known as cryptophthalmos-syndactyly syndrome

Related symptoms:

  • Intellectual disability
  • Microcephaly
  • Hypertelorism
  • Cryptorchidism
  • High palate


SOURCES: ORPHANET MENDELIAN

More info about FRASER SYNDROME

Low match ACROFACIAL DYSOSTOSIS, RODRÍGUEZ TYPE


Acrofacial dysostosis Rodriguez type is a multiple malformative syndrome in which mandibulofacial dysostosis and severe limb reduction defects are associated with complex malformations of different organs and systems especially the CNS, urogenital tract, heart, and lungs. The mandibulofacial defect, characterized by extremely severe microretrognathism and cleft palate, causes death by respiratory distress. Limb reduction is severe and includes shoulder and pelvis hypoplasia, phocomelia with humerus hypoplasia, absent radius and ulna, complete absence of long bones of the legs, and various hand anomalies, predominantly preaxial reduction (absent thumbs). Other features include CNS malformations (agenesis of corpus callosum and acqueductal stenosis), lung anomalies (absent lung lobulation), complex cardiac malformations, and unicornis uterus. These infants also show facial dysmorphism and ear anomalies. The condition is a rare with an autosomal recessive mode of inheritance. The prognosis is poor and this condition leads to death in utero or shortly after birth.

ACROFACIAL DYSOSTOSIS, RODRÍGUEZ TYPE Is also known as rodriguez lethal acrofacial dysostosis syndrome

Related symptoms:

  • Short stature
  • Hypertelorism
  • Micrognathia
  • Cleft palate
  • Low-set ears


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about ACROFACIAL DYSOSTOSIS, RODRÍGUEZ TYPE

Low match RAPP-HODGKIN SYNDROME; RHS


RAPP-HODGKIN SYNDROME; RHS Is also known as ectodermal dysplasia, anhidrotic, with cleft lip/palate

Related symptoms:

  • Short stature
  • Hearing impairment
  • Micrognathia
  • Cleft palate
  • Ptosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about RAPP-HODGKIN SYNDROME; RHS

Top 5 symptoms//phenotypes associated to Breast carcinoma and Finger syndactyly

Symptoms // Phenotype % cases
Syndactyly Common - Between 50% and 80% cases
Wide nasal bridge Common - Between 50% and 80% cases
Cleft palate Common - Between 50% and 80% cases
Toe syndactyly Uncommon - Between 30% and 50% cases
Hypodontia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Breast carcinoma and Finger syndactyly. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Ectodermal dysplasia Midface retrusion Cleft upper lip Cleft lip Intellectual disability Micrognathia Malar flattening Wide intermamillary distance Nail dysplasia Oral cleft Hypohidrosis Protruding ear Dystrophic toenail Abnormality of dental morphology Prominent nasal bridge Neoplasm Hypogonadism Abnormality of the ear Seizures Ectrodactyly Bilateral single transverse palmar creases Hyperlordosis Thin skin Microdontia Hypertelorism Short stature Hypotrichosis Alopecia Sparse hair Bilateral cleft lip and palate Clinodactyly Dystrophic fingernails Scrotal hypoplasia Conductive hearing impairment Pili torti Clinodactyly of the 5th finger Sparse eyelashes Depressed nasal bridge Abnormality of dental enamel Sparse and thin eyebrow Abnormality of cardiovascular system morphology

Rare Symptoms - Less than 30% cases


Narrow mouth Pulmonary hypoplasia Underdeveloped nasal alae Anal atresia Palmoplantar hyperkeratosis Cutaneous finger syndactyly Nail dystrophy Camptodactyly Hyperhidrosis Abnormality of the ureter Abnormality of the dentition Supernumerary nipple Lacrimal duct stenosis Abnormal hair pattern Sparse lateral eyebrow Carious teeth Fine hair Recurrent respiratory infections Neurological speech impairment Synophrys Bilateral cleft lip EEG abnormality Macrotia Abnormality of the philtrum Progressive hypotrichosis Downslanted palpebral fissures Sparse scalp hair Anodontia Highly arched eyebrow Bifid uvula Lacrimal duct atresia Hypoplastic nipples Cutaneous syndactyly of toes Split hand Hypospadias Split foot Low-set ears Microcephaly Radioulnar synostosis Abnormality of pelvic girdle bone morphology Global developmental delay Abnormal form of the vertebral bodies Dental malocclusion Hypoplasia of the maxilla Single transverse palmar crease Microtia Hallux valgus Low-set, posteriorly rotated ears High forehead Posteriorly rotated ears Narrow nose Cryptorchidism Brachydactyly Ptosis Triphalangeal thumb Hearing impairment External ear malformation Generalized hyperpigmentation Anal stenosis Encephalocele Dental crowding Ankyloblepharon Multicystic kidney dysplasia Atresia of the external auditory canal Anophthalmia Hypohidrotic ectodermal dysplasia Vertebral segmentation defect Abnormal lung lobation Renal hypoplasia Myelomeningocele Tracheal stenosis Calvarial skull defect Ectopic anus Bifid tongue Bicornuate uterus Vaginal atresia Abnormal vagina morphology Subglottic stenosis Laryngeal stenosis Omphalocele Hypoplasia of penis Hyperconvex nail Anhidrosis Progressive alopecia Small, conical teeth Submucous cleft soft palate Abnormal facial shape Sensorineural hearing impairment Pili canaliculi Pterygium Scaling skin Absent lacrimal punctum Anteverted ears Anhidrotic ectodermal dysplasia High palate Blindness Hyperconvex fingernails Microphthalmia Strabismus Umbilical hernia Scoliosis Trichodysplasia Velopharyngeal insufficiency Ambiguous genitalia Abnormality of the middle ear Female pseudohermaphroditism Submucous cleft hard palate Deep-set nails Conical tooth Abnormality of the uterus 11 pairs of ribs Hypoplastic labia majora Aqueductal stenosis Hand oligodactyly Phocomelia Arrhinencephaly Aplasia/Hypoplasia of the ulna Absent forearm Sprengel anomaly Ventricular septal defect Delayed eruption of teeth Palmoplantar keratoderma Small nail Recurrent otitis media Renal dysplasia Widely spaced teeth Coarse hair Abnormality of the voice Non-midline cleft lip Short tibia Thick nail Urethral atresia Coloboma Cryptophthalmos Cleft ala nasi Wide pubic symphysis Lacrimal duct aplasia Midline nasal groove Malformed lacrimal duct Intrauterine growth retardation Talipes equinovarus Flexion contracture Deeply set eye Short philtrum Dry hair Prominent nose Wide anterior fontanel Microretrognathia Renal hypoplasia/aplasia Overlapping toe Cystic renal dysplasia Short humerus Oligodactyly Aplasia/Hypoplasia of the radius Fibular hypoplasia Shallow orbits Abnormality of the skeletal system Hypertension Epiphora Prominent crus of helix Renotubular dysgenesis Partial duplication of the distal phalanx of the 3rd finger Partial duplication of the distal phalanx of the 2nd finger Absent first metatarsal Cleft of chin Long nose Delayed cranial suture closure Broad hallux Open bite Trigonocephaly Premature closure of fontanelles Dry skin Abnormality of the genitourinary system Increased intracranial pressure Sleep apnea Cutaneous syndactyly Eczema Plagiocephaly Cutaneous photosensitivity Narrow palate Inflammatory abnormality of the skin Proximal radio-ulnar synostosis Duplication of the distal phalanx of hand Elbow flexion contracture Lambdoidal craniosynostosis Abnormality of the skull Coronal craniosynostosis Short columella Abnormality of the antihelix Blepharospasm Adrenal hyperplasia Abnormality of digit Buphthalmos Oxycephaly Anterior plagiocephaly Vertebral fusion Deviated nasal septum Craniofacial dysostosis Neoplasm of the breast Congenital adrenal hyperplasia Parietal foramina Abnormal nasolacrimal system morphology Flat forehead Adrenogenital syndrome Craniofacial asymmetry Mild hearing impairment Narrow internal auditory canal Skull asymmetry Coxa valga Abnormality of the face Epicanthus Intellectual disability, moderate Primary amenorrhea Joint contracture of the hand Hypergonadotropic hypogonadism Gonadal dysgenesis Ovarian neoplasm Flat face Facial asymmetry Broad forehead Abnormality of the kidney Craniosynostosis Telecanthus Migraine Mandibular prognathia Triangular face Proptosis Brachycephaly Abnormal dermatoglyphics Abnormal heart morphology Brittle hair Aplasia/Hypoplasia of the eyebrow Optic atrophy Hypoplasia of the zygomatic bone Amenorrhea Convex nasal ridge Skin ulcer Alopecia of scalp Abnormality of the nail Finger clinodactyly Conjunctivitis Oligodontia Dermal atrophy Melanocytic nevus Low anterior hairline Freckling Amblyopia Broad thumb Fair hair Adermatoglyphia Generalized hypopigmentation Sparse axillary hair Absent nipple Breast hypoplasia Nasolacrimal duct obstruction Toenail dysplasia Fingernail dysplasia Nail pits Hypotelorism Conical incisor Premature loss of permanent teeth Decreased number of sweat glands



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Ptosis and Long face, related diseases and genetic alterations Spasticity and Toe syndactyly, related diseases and genetic alterations Cleft palate and Proximal muscle weakness, related diseases and genetic alterations Abnormal facial shape and Sparse scalp hair, related diseases and genetic alterations Generalized hypotonia and Hepatitis, related diseases and genetic alterations Neoplasm and Heterotopia, related diseases and genetic alterations Microphthalmia and Wide intermamillary distance, related diseases and genetic alterations

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